| Regulatory Affairs Officer This leading and well respected pharmaceutical company with 45 offices worldwide has an exciting vacancy for an experienced Regulatory Affairs Officer in the Greater London area. The position involves preparing and submitting UK licence applications, variations, and renewals. It also involves assisting with tender applications to support company export activity as well as liasing with regulatory bodies, third party suppliers, manufacturers, and other company departments. To be considered for the post, you will need experience of the pharmaceutical industry and regulatory affairs, a chemistry or life science degree, and computer proficiency in Word and Excel. Your personal qualities are as important as your technical background, and you shou | |
| Formulation Scientist A global technology company are looking to appoint a new Formulation Scientist to provide the skills to support project team activity for all aspects of inhalation product development in alignment with overall business objectives. We are currently looking to recruit a Formulation Scientist to provide the skills to support project team activity for all aspects of inhalation product development in alignment with overall business objectives. The company is a $21 billion global technology company, who are continuously finding new ways to make amazing things happen. Inspired by working closely with our customers, we create innovative products that help make the world smarter, faster, healthier and safer. Salary: Circa £23,000 per annum Key resp | |
| Electrical / Instrument Technician A Pharmaceutical Manufacturer seeks an Electrical/ Instrument Technician. You will be required to fault find and repair all types of electrical and instrumentation equipment and systems to ensure that plant downtime is kept to a minimum, effectively prioritise jobs. Suitable candidates will have an approved apprenticeship or equivalent. A Pharmaceutical Manufacturer seeks an Electrical/ Instrument Technician. You will work within the Maintenance/Environmental Operations Team to act as the first point of contact and provide the site with around the clock instrument and electrical breakdown support. To carry out this role the job holder will be required to fault find and repair all types of electrical and instrumentation equipment and systems | |
| Mechanical / Electrical Designer A Pharmaceutical Manufacturer seeks a Mechanical/ Electrical Designer. You will produce preliminary schemes and complete design/ detail drawings for both new and existing plant buildings. Suitable Candidates will have an ONC, HNC or equivalent and general engineering experience in a particular discipline, preferably in a Primary Pharmaceutical environment. A Pharmaceutical Manufacturer seeks a Mechanical/ Electrical Designer. You will produce preliminary schemes and complete design/ detail drawings for both new and existing plant and plant buildings necessary for Fine Chemical manufacture. On occasions, the designer may assume the role of "Project Engineer" for the management and execution of small projects which are suited to his/ her area | |
| Senior Regulatory Writer A Medical Writer is sought to carry out regulatory and drug safety medical writing activities to the highest possible standards for pharmaceutical companies. The Person: This is a position for a very experienced (at least 4 years in a pharmaceutical and/or CRO environment) and competent regulatory and/or drug safety medical writer who has in-depth knowledge, and exemplary writing and quality control experience, of a wide range of regulatory / drug safety documentation such as: Common Technical Documentation (including Module 2:2.5, 2.7 and Module 5. Knowledge of non-clinical documentation would also be an advantage); Clinical Study Reports and protocols of all phases; investigator's brochures; US IND; and safety documentation including: per | |
| Pharmacists for New Zealand Do you want to develop your professional career while enjoying the benefits of life in New Zealand's cosmopolitan island paradise? Discover the diverse culture and outdoor lifestyle in our great country. We have opportunities from Queenstown to Auckland with one of New Zealand's fastest growing companies for experienced pharmacists with a commitment to client focused care and education. Move permanently or take a career break, we can assist you whatever your plans are! Advice on registration, visas, accommodation and everything you need to make this happen!! Available on request. Benefits: Contact: Lee Keegan Further info: | |
| Regulatory Affairs My client is an established Pharmaceutical company and is looking to hire regulatory affairs staff at all levels. If you operate within this sector then we have a number of openings and clients who will be interested in you, please drop me a line by email or call me 02392 322 322 chutchings@strgroup.co.uk Benefits: Contact: Further info: Full Time | |
| Locum Pharmacist Locum Pharmacist in the North West Required Urgently Dispensary & ward pharmacist required for this popular hospital to start in January. Candidates must have UK hospital experience and two references. Accommodation is available on site. Benefits: Contact: Further info: Full Time | |
| Clinical Pharmacist 2 x Locum Clinical Pharmacists Required, Band 7 or 8 Hospital requires two locums to start early January for at least three months. Candidates must have UK hospital experience and have worked on wards and in dispensary. Chemotherapy experience would be a big advantage. Accommodation is available on site. Benefits: Contact: Further info: Full Time | |
| Pharmacists Excellentopportunities to work and travel in Ireland! Are you a UKhospital pharmacist? Are you looking for a new opportunity? We have some fantastic hospital roles based in Irelandto which we are currently recruiting. Weâ??re looking to find registeredPharmacists; and currently have roles available in all areas of specialisation. These are temporary roles and so will attract competitiverates of pay, and we will offer good benefits packages. We can also help withsupport throughout your placement; including help with accommodation. For further information, please apply today for moredetailsâ?�. Benefits: Temporary Contact: Bianca WintRecruiter: Labmed Further info: | |
| Data Manager Are you looking for new challenges? Would you like to change the way we treat diabetes? We are expanding our team and looking for a Data Manager to join our Clinical Research department and successfully help run our large international phase 3 programme, iINHALE. Our new inhaled insulin will change how we deliver insulin and make a difference in the lives of the growing number of people living with diabetes. This is your unique opportunity to support Novo Nordisk A/S leadership in diabetes and join an eager Clinical Team of Data Managers, International Trial Managers, Clinical Trial Administrators, Statisticians and Medical Writers and make alternative insulin administration a reality at Novo Nordisk A/S! Challenges In your position as a Da | |
| Pharmacy Technician We are currently looking for a PharmacyTechnician for a hospital based in the North East of Ireland, close to Dublin.We need to find someone who has had previous experience within a hospitalenvironment, and can show a proven track record working as a pharmacytechnician. We can help with accommodation if required, and can offeryou an excellent rate of pay; dependant upon your experience. For furtherinformation, regarding this post, please apply todayâ?� Benefits: unspecified Contact: Bianca WintRecruiter: Labmed Further info: | |
| Band 7 Upper / Lower Pharmacist (B / C Grade Pharmacist) Do you have previous ENT experience? We are looking for an ENT Pharmacist to start in an ongoing position from 22 December 2006. This is an excellent opportunity for a UK Registered Pharmacist to gain further London based experience. The hourly rate on offer for this position is between £21.58 and £24.05 as Ltd Company. Please apply today for further information�. Benefits: Temporary Contact: Craig KayserRecruiter: Labmed Further info: | |
| Formulation Scientist Our world class client is looking for a formulation scientist to provide the skuills to support project team activity for all aspects of inhalation product development in alignment with overall business objectives Benefits: Permanent Contact: Toneya SarwarRecruiter: Jobs@pertemps Further info: | |
| Health and Safety Officer - Radiation We currently have an opportunity for a Health and Safety professional that has experience in chemical/ radiological/ biological industries. You will be working for a well established company with 450 staff acting as the H&S Officer as well as the radiation Officer. The job will involve maintaining safety records, offering advice and training staff. A major part of your role will be looking at controls of radiation coming onto site including safe use, handling, storage, security and disposal of radioactive waste. You will be based in Newbury with occasional local travel. Qualifications required are the NEBOSH Certificate or NEBOSH Diploma and relevant work experience. Hours will be 37/ week Mon - Fri. Salary is between £23k - £32k depe | |
| Lead Mechanical Engineer A Pharmaceutical Manufacturer seeks a Mechanical Engineer to lead the mechanical equipment standards and maintenance strategies for the site. Suitable applicants will hold a degree or equivalent in an appropriate engineering discipline. You will hold experience in a process manufacturing environment. A Pharmaceutical Manufacturer seeks a Mechanical Engineer to lead the mechanical equipment standards and maintenance strategies for the site. Key result areas will include; to define 'site driven' maintenance strategy; to develop and define maintenance routines are in place for all items of equipment; to develop and define CBM techniques; to define the procedures to ensure compliance with statutory/compliance legislation with regards to vessel | |
| Top 10 Pharmaceutical Company - Clinical leader, Edinburgh £50-60k + bens Unique opportunity with leading pharmaceutical company to become actively involved in achieving cost-effective research and development across the globe. My client is looking for a commercially minded medical professional with a passion for medical advancement and proven expertise in clinical research. This role enables you to demonstrate your line management skills as well as your ability to work in a target-driven fast-paced environment in a world-leading company, renowned for its unrivalled t : Unique opportunity with leading pharmaceutical company to become actively involved in achieving cost-effective research and development across the globe. My client is looking for a commercially minded medical professional with a passion for medica | |
| Scientific Sales Specialist Scientific Sales Specialist: A progressive and ambitious company, selling various instrumentation / disposables into the Pharmaceutical & Life Science sectors, looking for an experienced Scientific Sales Specialist. The company specialises in Rapid Microbiology & Process Analytical Testing particularly Microbial Detection, Microbial Identification, BioBurden Analysis, Decontamination and Sanitization, and Calibration of Liquid Handling systems and Pipettors. Previous sales experience essential This is an exciting opportunity during the early days of this exciting new company. They are looking for: * an experienced Scientific Sales Specialist, with * a lab background, preferably Microbiology, and * a strong desire to acheive in Sales. Salary | |
| Clinical Project Manager Phase I-IV, all medical areas Winchester £50k With experience in project/data management and clinical research, you will become involved all phases and all cutting-edge medical areas (oncology, CNS, cardiovascular etc.) Leading CRO is offering the opportunity in project management of the entire life-cycle of local and global clinical studies. Abraxas plc acts as an employment agency/business. No terminology in this advert is intended to discriminate on the grounds of age, and we confirm that we will gladly accept applications from perso : With experience in project/data management and clinical research, you will become involved all phases and all cutting-edge medical areas (oncology, CNS, cardiovascular etc.) Leading CRO is offering the opportunity in project management of the entire l | |
| Line Manager, Manage and motivate clinical staff at large pharma Middx This is a great opportunity for a clinical professional that looks to exploit their managerial and motivational skills in a clinical setting. You will get the opportunity to develop your line-management skills at a leading pharma company with excellent career progression opportunities. As a clinical line manager, you will get the chance to manage the performance, development and growth of clinical research associate (CRA) teams, as well as provide clinical consultation to project teams. Abraxas : This is a great opportunity for a clinical professional that looks to exploit their managerial and motivational skills in a clinical setting. You will get the opportunity to develop your line-management skills at a leading pharma company with excel | |
| Analytical Chemist-Top 10 Pharma Co-Kent-£Competitive Are a recent graduate looking for your first role in the Pharmaceutical industry or are you an experienced Analytical Chemist looking for new challenges and the chance of real career progression. A top 10 Pharmaceutical company globally is looking for and Analytical Chemist to come in to support the company's technical operations functions. You will be resolving analytical issues associated with commercial, research and development API's and drug products. Gain experience in providing technical : Are a recent graduate looking for your first role in the Pharmaceutical industry or are you an experienced Analytical Chemist looking for new challenges and the chance of real career progression. A top 10 Pharmaceutical company globally is looking | |
| Clinical Project Manager, Leading CRO Winchester £50k Leading CRO is offering the opportunity to become involved in project management of local and global clinical studies in several therapeutic areas. Abraxas plc acts as an employment agency/business. No terminology in this advert is intended to discriminate on the grounds of age, and we confirm that we will gladly accept applications from persons of any age for this role. : Leading CRO is offering the opportunity to become involved in project management of local and global clinical studies in several therapeutic areas. The company is undergoing growth and is looking for a clinical professional who can progress within the company as a line-manager or senior program manager. The ideal candidate has experience in either data management or clini | |
| CRAs, Senior CRAs and Principal CRAs required! We have vacancies for CRAs, Senior CRAs and Principal CRAs in office and field-based locations throughout the UK. Candidates should have at least 12 months experience working as a CRA or study monitor, plus a life sciences degree, driver's licence and valid passport. Our client is a leading global Contract Research Organisation providing discovery, development and post-approval services to their wide range of clients - pharmaceutical, biotechnology, medical device, academic and government organisations. With offices in more than 25 countries they apply innovative technologies, therapeutic expertise and a commitment to quality to help their clients and partners maximise returns on their R&D investments and accelerate the delivery of safe and | |
| Formulation Scientists Formulation Scientists, Ref: 13862 MC Our East Midlands based client develops and manufactures a range of pharmaceutical products. They are actively looking for Formulation Scientists to provide support to the new product development teams. Duties for these positions will include: - - Performing physical testing of pharmaceutical products for stability and development studies / batch release activities - Development and maintenance of specifications and regulatory submission activities - Stability database management - Assess and recommend new improved methods, equipment and processes for the processing of formulation components - Assist in the transfer of laboratory scale processes to the Process Development and Technology group Applicatio | |
| Mechanical Production Engineer Qualified Mechanical Production Engineer required ASAP in Oxfordshire for Company which makes human inplants. This is a high volume-manufacturing environment, which requires an experienced production engineer who would ideally come from a medical, or pharmaceutical industry. This is an industry, which is highly dominated by manufacturing procedures and forward thinking philosophies. Typical day-to-day duties will include working closely with the design and development teams in the development of their product range. In addition, quality procedures play a big part of the job, so working on ways to instil these procedures on the shop floor is essential. Experience required in: electronics and or mechanical engineering, designing specialist eq | |
| Pharmacy Techician required - Southampton Medical Recruitment Specialists require a Dispensing Technician for a busy Pharmacy located close to the centre of Southampton. This is a full time position and duties will include helping in the dispensary and giving advice on OTC products to customers. The ideal candidate for this position will have a recognized qualification such as an NVQ level 2 or 3 and have had some previous experience of working in a high volume environment. The salary and benefits package for this position is negotiable ? for further information please call Stephen Whyte at Medical Recruitment Specialists. Benefits: Salary and benefits package negotiable Contact: Stephen Whyte Further info: | |
| PHARMACY TECHNICIAN (DUBLIN) In joining this compassionate team of healthcare professionals, the successful candidate will be joining a team who strive for an environment providing quality service while respecting the unique dignity of each patient and working strongly together to ensure fairness in the workplace. This organisation provides good working hours and generous annual leave as well as extras such as pension scheme, VHI scheme and subsidised meals. Responsibilities: ? Participate in dispensing individual prescriptions for patients and staff. ? Dispensing and maintenance of Medications. ? Dispensing and maintenance of MDA controlled drugs. ? Participate in compounding extemporaneous products. ? Participate in the day to day work in an aseptic production unit. | |
| Pharmacist Manager - Worcestershire Medical Recruitment Specialists require a Pharmacist for a full time position based in the north Worcestershire area. This role is based in a high volume environment in a Pharmacy that delivers MUR?s, EHC, Smoking Cessation counseling and blood pressure testing in line with the new contract. Newly registered Pharmacists are encouraged to apply as full support will be provided initially from an experienced team of made up of 2 technicians, 2 OTC staff and a Retail Manager. The ideal candidate for this role will be keen to progress their career within Retail Pharmacy by working closely with local GP practices and members of the local Community. The successful candidate will receive a generous salary and benefits package which includes a struc | |
| Head of Regulatory Affairs, London Pharmaco Head of Regulatory Affairs, London Pharmaco My client is a small, rapidly expanding Pharmaceutical company based in central London, who have recently floated on the stock market. They are looking for a Head of Regulatory Affairs to aid their expansion. The role involves: -supporting, co-ordinating, preparation and following through submissions -being the key point of contact for regulatory authorities -defining regulatory procedures and strategies -keeping abreast of developments and changes in regulations, and communicating these to staff. The successful candidate will require: -strong Pharmaceutical Regulatory Affairs experience -experience of European submissions -a good knowledge of UK and European legislation -a proven track record in | |
| Global Pharmaco, Buckinghamshire, seek a Regulatory Affairs Associate Global Pharmaco, Buckinghamshire, seek a Regulatory Affairs Associate This world-renowned pharmaceutical company, based in Oxfordshire, are looking for 2 Regulatory Affairs Associates. The positions involve: -gaining regulatory approval for marketing authorisations and new pharma products -maintaining existing authorisations -providing regulatory support and advice to commercial divisions -liaising with global R&D The successful candidate must have: -at least 3 years Regulatory Affairs experience -experience of European Regulatory bodies Experience of MMP, MRP, and full project lifecycle would be a bonus. This is an excellent opportunity for the successful candidate to join one of the world's leading Pharmaceutical company during a growth p | |
| Cambridgeshire // Regulatory Affairs Officer Cambridgeshire // Regulatory Affairs Officer My client is part of a worldwide association of independent pharmaceutical companies that have been developing new drugs for more than half a century. They are currently looking for a Regulatory Affairs Officer for their site in Cambridgeshire. The role involves: -liaison with Worldwide Drug Safety and Pharmacovigilance and relevant project teams regarding the preparation, revision, review and issue of Company Core Data Sheets -maintenance of Company Core Data Sheets in the Regulatory Affairs document management system monitoring of compliance of Summary of Product Characteristics with Company Core Data Sheets across the associated companies in Europe -assistance in the preparation of Summary of | |
| Regulatory Associate II, Germany Regulatory Associate II, Germany My client is part of a global group of development companies, who specialise in conducting clinical research for the Pharmaceutical, Biotechnology and Medical Device industries, from Phase I through to post-marketing. They are currently looking for a Regulatory Associate for their site in Frankfurt. The role will involve: -review of regulatory documentation for clinical trials -compilation of submissions (INDs, CTAs, NDAs, and MAAs) -conducting of Quality Control reviews of regulatory documents such as Clinical Study Reports -keeping up to date with regulatory requirements, ICH guidelines, Good Clinical Practice, and SOPs. The successful candidate requires: -a Bachelor's degree in a life science, or equivale | |
| Pharmaceutical company//Scotland//Head of Regulatory Affairs Pharmaceutical company//Scotland//Head of Regulatory Affairs My client is a rapidly growing Pharmaceutical company, based in Scotland, who focus on secondary care markets. They are currently looking for a Head of Regulatory Affairs. The role will be a hands on one, and a lot ofstrategic work will be involved. There would be a heavy focus on the early phases of clinical trials, and on working to European standards. The successful candidate will have previous big Pharma experience, ideally with Director-level experience. They will have proven Regulatory Affairs managerial skills, and a PhD. This is an excellent opportunity to join a rapidly expanding company at the ground level, with strong prospects for advancement. The salary is excellent, | |
| Central London location // Head of Regulatory Affairs Central London location // Head of Regulatory Affairs My client is a small Pharmaceutical company based in central London, who have recently floated on the stock market. They are looking for a Head of Regulatory Affairs to aid their expansion. The role involves supporting, coordinating, preparation and following through submissions, being the key point of contact for regualtory authorities, defining regulatory procedures and strategies, keeping abreast of developments and changes in regulations, and communicating these to staff. The successful candidate will require strong Pharmaceutical Regulatory Affairs experience, experience of European submissions, a good knowledge of UK and European legislation, and a proven track record in successful | |
| Experienced Clinical Research Candidates needed! Excellent opportunities and competitive salaries for roles across the UK and Europe. If you are a CRA, SCRA or Project Manager and looking for a new challenge or your situation has changed then please call or send your CV to be short-listed against suitable and relevant roles to fit your requirements. Contact Lizzy May at Real Pharma for advice on 0207 434 7999 or attach your CV now. Are you a Clinical Research Associate, Senior Clinical Reseach Associate, Clinical Project Manager, Project Director, CTA? whatever your level or area of expertise. If you are considering your options, then please call for an informal discussion. (Real IT Resourcing Limited acts as an Employment Agency and an Employment Business) Benefits: Permanent Contact: | |
| Clinical Research Associate ? Biotech Company ? South East ? c 25k Clinical Research Associate urgently required to join an internal drug discovery and development team within a successful biotechnology company. The company?s primary focus is Oncology. Your role will cover the site selection, initiation, assessment and close out of sites. Responsibilities will include thorough clinical study monitoring and management, working closely with senior managers to implement new development plans. Candidates must possess: - 3-5 years experience as a CRA in a pharm/biotech/CRO environment. - Or life sciences background and relevant academia - Oncology experience and management an advantage! - Ability to travel in the UK and abroad - Strong managerial and personable skills This is an exciting and challenging role wi | |
| Clinical Project Manager, Oncology, South East Clinical Project Manager urgently required to join a global Biotech company in the South East. This company is one of the largest, longest standing biotech companies with an excellent reputation worldwide. This company develops novel products and has created some groundbreaking drugs in the pharmaceutical market. You will be part of the Oncology team, acting as a study manager. Candidates will have a few years commercial experience as project manager with oncology being your main therapeutic area of experience. This global company gives the opportunity for training and development, career progression and travel experience. Relocation help is available and they encourage diversity and innovative ideas. Contact Lizzy May at Real Pharmaceutica | |
| Clinical Project Manager, Cambridgeshire, >£50,000 Clinical project manager urgently needed to join a global pharmaceutical company in Cambridgeshire. This pharmaceutical company specialises in oncology and is looking for an experience clinical project manager to manage the clinical team on Phase I+II clinical trials. Candidates must possess a strong educational background with at least 3 years experience as a clinical project manager from either a CRO/Pharmaceutical or Biotech background. You will ideally have experience in Oncology but this not essential, but the desire to gain this therapeutic experience is important. Contact Lizzy May at Real Pharmaceutical for more information on 0207 434 7999 or apply to this role now. (Real IT Resourcing Limited acts as an Employment Agency and an Em | |
| Senior Clinical Research Associate, North West. Senior CRA urgently needed to join a leading CRO in the North West. As Senior CRA you will be responsible for the Co-ordination of the setting up, running and reporting of clinical trials from inception to reporting and publication of results. You will assess and select the external clinical trial sites, produce and co-ordinate the production of clinical trial plans, protocols, CRFs and all trial related paperwork. Candidates will ideally have at least 3 years experience as a Senior CRA within a pharmaceutical or CRO environment. This in an excellent chance to develop your commercial research experience with the opportunity for career progression to project management status. The salary for the role is £30,000. Contact Lizzy May at Real | |
| Regulatory Affairs Officer, Cambridgeshire, Pharmaceutical Company Regulatory Affairs Officer, Cambridgeshire, Pharmaceutical Company My client is part of a worldwide association of independent pharmaceutical companies that have been developing new drugs for more than half a century. They are currently looking for a Regulatory Affairs Officer for their site in Cambridgeshire. The role involves liaison with Worldwide Drug Safety and Pharmacovigilance and relevant project teams regarding the preparation, revision, review and issue of Company Core Data Sheets, maintenance of Company Core Data Sheets in the Regulatory Affairs document management system, monitoring of compliance of Summary of Product Characteristics with Company Core Data Sheets across the associated companies in Europe, assistance in the prepa | |
| Global Pharmaco // Berkshire // QA Specialist Global Pharmaco // Berkshire // QA Specialist One of the world's leading Pharmaceutical developers and manufacturers is looking for a Quality Assurance (QA) Specialist. The role involves extensive travel and GCP auditing of the companies R&D projects, maintaining and implementing Quality systems, and training the company's staff in the area of Quality. The successful candidate must have strong Quality Assurance auditing experience in a GCP environment, good experience of SOPs, and good IT skills. Communication, negotiation, and problem-solving skills are also integral to the role. This is an excellent opportunity for the successful candidate to join one of the world's leading Pharmaceutical company during a growth period, so career opportun | |
| Senior QA Auditor required, Middlesex Senior QA Auditor required, Middlesex My client is one of the world's leading Pharmaceutical Contract Research Organisations, with sites worldwide. They offer excellent training and career opportunities, as well as an excellent working environment. The role involves planning and conducting internal and external audits, mentoring of less experienced auditors, following up on multiple tasks and projects, handling of confidential information, liaising with QA management and staff, providing direction and coordination for project activities, and providing advice on regulatory compliance. The successful candidate will have a Bachelor's degree or equivalent experience, at least 5 years experience in the Pharmaceutical industry including 3 years o | |
| Clinical Project Co-ordinator, London, Pharma Clinical Project Co-ordinator urgently needed to join a Pharmaceutical Company in London. Our client is looking for experienced clinical project co-ordinators who have gained valuable experience within a CRO/Pharma environment. Candidates will have Project Management skills and excellent attention to detail. Strong educational backgrounds are essential as is the determination to progress to Clinical Project Manager level. Our client has successfully won new projects and this is how the vacancy has arisen-sheer success and natural growth. If you or a friend or colleague are interested in this position, please contact Lizzy May at Real Pharma or 0207 434 7999 to find out more details or apply to this role now! Clinical Project Co-ordinator ur | |
| Pharmaceutical company // Scotland // Head of Regulatory Affairs Pharmaceutical company // Scotland // Head of Regulatory Affairs My client is a rapidly growing Pharmaceutical company, based in Scotland, who focus on secondary care markets. They are currently looking for a Head of Regulatory Affairs. The role will be a hands on one, and a lot of strategic work will be involved. There would be a heavy focus on the early phases of clinical trials, and on working to European standards. The successful candidate will have previous big Pharma experience, ideally with Director-level experience. They will have proven Regulatory Affairs managerial skills, and a PhD. This is an excellent opportunity to join a rapidly expanding company at the ground level, with strong prospects for advancement. The salary is excell | |
| Clinical Research Associates/CRA?s, Oncology, Midlands, Pharma Clinical Research Associates required to join a Global Pharmaceutical company based in the Midlands. This company are a leading global pharmaceutical company built on a heritage of 150 years of quality. They specialise in injectable oncology products and have recently won new projects within Oncology. Candidates will ideally have CRO/Pharma background and Oncology experience will be ideal. As Clinical Research Associate your responsibilities will include organising study design and set up, Protocol development, IB development, CRF and Informed consent development, Interaction with Key opinion leaders, Site evaluation and selection, Trial timelines and budget management. This role is office based and generous benefits are on offer in return | |
| ONCOLOGY SENIOR CLINICAL PROJECT MANAGER, BERKSHIRE This role reports into the Clinical Project Director within a Global CRO. It will be your responsibility to manage oncology trials, prepare and/or reviews protocols and other study documentation as required by the Sponsor and in collaboration with the Medical Writing department. It will be your responsibility to designs and develop the Case Report Form, Design and develop clinical trial documents such as Project Plans and monitoring guidelines. You will oversees all aspects of study site management to ensure a high quality of data is generated by Investigative sites, resulting in consistently low query levels. Candidate will be educated to degree level and will have experience within clinical research, in particular Project Management withi | |
| Clinical Research Associate, CRO, Germany. Clinical Research Associate/CRA required to join a successful CRO in Germany. Our client have won new projects within Endocrinology, Oncology and RA. Candidates will be experienced CRA?s having worked within these therapeutic areas ideally. You will also have a strong educational background with a scientific background and passion for clinical research. The salary is between â?�35,000 and â?�45,000. If you are interested in this vacancy or think you may have a friend or colleague who may be, please call Lizzy May at Real Pharma on 0207 434 7999 or apply to this role now! Clinical Research Associate/CRA required to join a successful CRO in Germany. keywords: CRA, Clinical Research Associate, Clinical, Endocrinology, Germany (Real IT Re | |
| Clinical Research Associate, Phase 1, Pharmaceutical, London Clinical Research Associate required to join a Global Pharmaceutical company in the South East. It will be your responsibility to work in a field based capacity as part of the UK Phase1 team to manage phase I trials in Clinical Research Organisations (CROs) across London. Initially the position will involve undertaking all aspects of site management from initiation to close down. The CROs are within the London area but a flexible approach to travelling is required. Candidates will have strong Scientific backgrounds, a minimum BSc or nursing qualification, knowledge of ICH-GCP and the career drive to become a SCRA. The successful candidate will have -The ability to prioritise activities, -Demonstrate good communication skills, -Be familiar w | |
| Field based CRA?s, UK, Excellent Package! Clinical Research Associates urgently needed to join an established and successful CRO based in the South East. You will be field based, monitoring clinical trial sites across the UK. Your location will influence which sites you will be assigned. You will be working in a field based/home based capacity monitoring Phase III studies in Oncology. Candidates that have an oncology background = great! Those that don?t but would like to gain experience within this area, read on. Candidates will need to be advanced CRA?s, have a minimum BSc, have a full driving license and have an enthusiasm for all areas of clinical research. Candidates that have have LREC and MREC experience will be at an advantage. The salary for the role is negotiable on experi | |
| Clinical Research Associate South East Urgent Clinical Research Associate urgently needed to join a CRO in the South East. You'll be joining the world's leading CRO, responsible for the development of the world's top 30 best selling drugs. This organisation operates in over 30 countries.As a CRA you will ensure that clinical stages of research projects are completed in accordance to the clients needs. You will be responsible for initiating sites, assessing the clinical trials, monitoring and closing out of sites. You will have at least 1 year?s experience as a Clinical Research Associate within a Pharmaceutical or CRO environment. Contact Lizzy May at Real Pharmaceutical for more information on 0207 434 7999 or apply now. (Real IT Resourcing Limited acts as an Employment Agency and an | |
| Senior Clinical Data Manager, project responsibilities, Cambridgeshire An experienced Clinical Data Manager is needed by this Clinical Research Organisation to spearhead Clinical Data Management activities, including set-up and close, on a number of studies. This company is grounded in the present, although they have a firm perspective on where they want to be, and how you will fit in to their development plans. Your responsibilities will include: -the design and build of Oracle Clinical/ SAS and Excel databases -Training and mentoring junior staff in data review and validation -Co-ordination of coding with OC, data validation, EDC -Reviewing data management documentation and updating as necessary -Managing clinical data officers and Data entry clerks -Effectively communicating queries and issues between indiv | |
| Managing SAS Programmer, Yorkshire A leading Clinical Research Organisation are currently looking for Manager of SAS Programming to run a full body of Programmers at various levels. The ideal candidate will have a breadth of experience from clinical research environments, and will have expert knowledge of programming within clinical data. Preference will lie with those with at least 5 years of SAS programming experience, at least a BSc in a Scientific discipline, and some amount of managerial experience. Fundamental areas of your role are: -Problem solving programming problems in a consultative capacity -Training and mentoring -Overseeing career development plans and performing appraisals -Liasing with senior member of trial sponsors -Travel to other company offices -Ensurin | |
| Senior Clinical Research Associate-Multi-National CRO-Berkshire-30k Senior Clinical Research Associate urgently sought to support the Project Manager with day-to-day functional and organisational activities of international clinical trial management within a Multi-national CRO in Berkshire. Your role will be to act as a primary contact of the project team with study site personnel and ensure that the clinical trials are conducted in accordance with international regulatory and ethical guidelines for GCP. Your responsibilities will include assisting project management with the day-to-day running of international clinical studies. You will liase with CRA?s and Sponsors to track study progress, milestones, resolve logistical and practical issues and regulate quality standards, whilst maintaining an effective w | |
| Senior SAS Programmer, Reading This SAS Programming position is with a global CRO who are dedicated to client service. Working within a multi-disciplined team you will be ensuring the delivery of quality databases to meet client deadlines. While supporting other team members, you will be responsible for Clinical Database applications and SAS programming. You will also be involved with the Management of SAS issues. The ideal candidate shall be coming directly from another pharmaceutical company or CRO and have over three years experience in a clinical/ biometric/ biostatistical environment. This specialised, niche position is a waiting opportunity for those with the right qualifications and experience. This company shall reward your work with a highly competitive salary a | |
| Senior Clinical Research Associate, North Yorkshire, CRO Senior CRA urgently needed to join a Global CRO in North Yorkshire. By joining this successful global company you will be contributing toward the development of more-effective medical therapies that help save lives and improve the quality of life for millions of people around the world. In this clinical team you will be working on a variety of therapeutic areas on a range of trial phases. You will ideally have at least 18 months experience as a CRA, having worked in either a CRO/biotech or pharmaceutical company. You will ideally have a strong educational background, with a minimum bachelor?s degree qualification. The benefits are excellent and include private medical, dental and vision, an employee stock purchase plan, tuition reimbursemen | |
| SENIOR CLINICAL PROJECT MANAGER ? CRO ? SOUTH COAST Senior Clinical Project Manager urgently required to join a highly successful and global CRO based on the South Coast. The company specialises in clinical research, biometrics, interactive technologies, laboratory, clinical pharmacology and consulting services. As the worlds 4th largest provider of clinical trials, a recent survey of pharmaceutical and biotech companies rated the company as the markets ?favourite? Contract Research Organisation. Your role will be to effectively manage the activities of clinical studies and staff to meet targets and control costs. Responsibilities include managing projects to agreed timeframes and standards, keeping senior management informed of project status, quality and timelines. You will ensure training | |
| CLINICAL PROJECT MANAGER ROLE- MULTI-NATIONAL CRO-BERKSHIRE-c 55k Clinical Project Manager urgently required to manage and report international clinical trials for a Multi-national Contract Research Association in Berkshire. Your role will involve effective management of all aspects of clinical trials, including study preparations, initiations, monitoring and safety. You will liase with Sponsors and investigators with respect to consistency of protocol and trial progress. Your responsibilities will also include the evaluation of CRA?s and organising training courses for your colleagues. Candidates will possess: - Minimum 1-2 years at Senior CRA grade II level - At least 1-2 years at Project Manager grade II level - Experience in Project Manager Grade III duties - Excellent leadership skills This is a grea | |
| SAS Pharm Analyst role! The function of this new role is to support the Clinical Pharmacologists and Statisticians in the preparation of data in required biomedical formats. This would normally be from Excel spreadsheets into SAS datasets or other formats as requested. Need for some SAS programming experience but not extensive. Graduates with numerical degree plus one years experience in a pharmaceutical environment will also be considered. Successful candidates should have a relevant statistics, numerate or scientific degree together with some experience of SAS, an interest in data, attention to detail and quality as well as experience in or exposure to a pharmaceutical working environment. Need for good comminication and language skills Benefits: Contract Cont | |
| SAS SKILLED CANDIDATES FOR PHARMACEUTICAL ROLES OPPORTUNITIES TO WORK WITH MARKET LEADING PHARMACEUTICAL COMPANIES USING SAS FOR MODELLING, PROGRAMMING & DATA ANALYSIS. NEED FOR THOROUGH SAS SKILLS WITH 2+ YEARS PHARMACEUTICAL INDUSTRY TO WORK IN SENIOR POSITION AIDING RESPECTABLE WORLD LEADING FRIMS WITH DRUG DEVELOPMENT AND MEDICAL IMPLEMENTATION. THE ROLE INCLUDES ANALYSIS OF CLINICAL RESEARCH DATA USING SAS PROGRAMMES TO CREATE HIGHLY RESPONSIBLE MEDICAL STRATEGIES. NEED FOR SOME INDUSTRY EXPERIENCE. Benefits: Contract Contact: Natalie EffemeyRecruiter: Huxley Associates - London Further info: | |
| SAS Programmers Wanted in Pharmacy!!!!!! SAS programmers required for pharmaceutical roles in top UK healthcare companies. Programming, manipulating & implementing data from biomedical & clinical research to aid with drug development process. Need for 2 years + experience in SAS programming with 1 year + experience in the pharmaceutical arena to receive excellent bonuses & strong career progression. Benefits: Contract Contact: Natalie EffemeyRecruiter: Huxley Associates - London Further info: | |
| SAS Statistician - SAS, Clinical Trials - Interviewing Now SAS Statistician is needed by large pharmaceutical company to work on Phase III and Phase IV studies. The candidate will be familiar with logistic regression, non-parametric methods and writing statistical analysis plans. SAS programming of all analysis, tables, listings, appendices, figures (including graphs) and QC is also important. 5 yrs experience of working in a pharmaceutical or CRO background required.This has a high level of extending. For further information please submit your cv or contact Nick Gaisford at Pathway Datawarehousing (Pathway Resourcing Limited acts as an Employment Agency and an Employment Business) Benefits: Contract Contact: Nicholas GaisfordRecruiter: Pathway Further info: | |
| Quality Control Analysts Our client is a major manufacturer of pharmaceutical products and currently has a number of positions within their QC area for QC Analysts. You will be responsible for the analysis of raw materials, packaging components and intermediate and finished products, ensuring all work is documented, checked and reported promptly and that all cGMP/GLP regulations are strictly adhered to. A minimum HNC/HND or degree or similar and/or working experience as an analyst within a pharmaceutical environment is required. Entitlement to work in the UK is esssential. Please quote reference DH13290 in all correspondence. Benefits: Contact: Heather Deagle Further info: Full Time | |
| Product Testing Co-ordinator/Pharmaceuticals Our client is a major manufacturer of secondary pharmaceuticals based in the North East of England. They are seeking to appoint a Quality Control Co-ordinator within their Quality Operations area, supervising a team of 12 product testing analysts. This is a highly challenging role carrying responsibility for people management, quality compliance, health and safety, resource management and sample management. The successful candidate will be educated to degree level or degree calibre with experience of managing a team in a pharmaceutical laboratory environment. Knowledge or cGMP and regulatory requirements within the pharma industry is essential, together with planning and organising skills, a positive, "can do" approach and the ability to ma | |
| Senior Formulations Scientist Our client is a blue chip pharmaceutical research company, seeking to appoint a Senior Formulation Scientist. You will work on the development of dosage forms to client requirements, the transfer of these formulations to preclinical and clinical trials manufacturing areas and ensure that working practices comply with GLP/GMP standards. In addition to this you will prepare development protocols and reports and provide project progress information. You will also transfer formulation details of product to preclinical and clinical trials manufacturing personnel, prepare SOP's and assist with training. A relevant degree or equivalent level of technical competency is required, together with extensive experience of solid dose form and development, | |
| Shift Process Chemist Would you like to work for one of the North Easts' leading chemical companies as a Process Chemist? Do you thrive on project work and working on a pilot plant scale? SRG wants to hear from process chemists who wish to work for a team that is recruiting due to expansion. In return our client can offer a stimulating and responsible role for shift working chemists. Applicants will need to be qualified to degree level, or equivalent, in a Chemical Sciences subject. In addition you will have experience of working on a process plant, especially with exposure to heterogeneous catalysis, coupled with strong HPLC/GC skills. You will also have proven interpersonal and communication skills to liaise with internal and external customers. 'SRG is unable | |
| Lab Development Chemist LAB DEVELOPMENT CHEMIST - West Midlands SALARY �22-25K Are you a successful development chemist? Do you want to be involved in the day-to-day lab routine with a slant towards method development? Ideally you will have a good degree in Chemistry or equivalent with proven GC method development experience. Your main responsibilities: � Provide method developmental direction and supervision � Aid in the day to day analytical duties � Develop and enhance current analytical methods � Training of lab members in methodologies If you're an able developmental chemist with a completer-finisher attitude, then you're the one for me! So please apply online. hasina.begum@srg.co.uk 'SRG is unable to employ any candidates requiring a sponsorship to | |
| Quality Control Analyst - Shift Want to progress within the Pharmaceutical industry? This company is well established and going through a phase of steady growth. This is a great time to get on board! We are looking for a Quality Control Analyst to work on a shift basis (double days). You will analyse raw materials, intermediates and finished products following SOPs. On a daily basis you will use HPLC, GC, KF, wet chemistry and TLC. All work will be carried out to GLP and GMP. Entitlement to work in the EEA is essential. Please quote reference ST13294 in all correspondence. Benefits: Contact: Ajay Patel Further info: Full Time | |
| Opportunities in Pharma Sales Opportunities in Pharma Sales, various territories across the North East �22,000 - �30,000 + excellent benefits package No pharmaceutical experience, no problem. No ambition, no way. Does it take a certain kind of person to succeed in pharmaceutical sales? Yes. We need people who've achieved a lot in a short time. Who've made their mark in the most challenging commercial environments. Who are hungry to achieve more - much more. People, in short, like you. Does it take any previous experience of pharmaceuticals? Not round here. Tackling a steep learning curve, you'll soon be ready to build effective relationships with GPs and medical customers across your territory - driving the bottom line by promoting some of the most innovative drugs | |
| Statistician, GLOBAL PHARMACEUTICAL COMPANY, £25000 - £40000, South Ea This pharmaceutical company has an international atmosphere, and is looking to take on a career-minded statistician. With an emphasis on career development, support, and quality statistical analysis, this company is offering a springboard to experience and a pathway to an exceptional working environment. Your role will consist of planning statistical procedures within clinical trials, implementing and performing these techniques, and reporting your findings. Due to the level and technical difficulty of analysis involved my clients prefers candidates to hold an MSc or PhD in Statistics. With a MSc you should have two years of relevant experience, although you may be considered with less, otherwise a PhD will fully qualify you for this dynami | |
| Qualified Person/QP/Quality Assurance/Quality Compliance Summary There is an opportunity for a Qualified Person, who must be eligible for appointment as a qualified person to join a company in Sussex. Job Description The Company Represented is one of the largest generic pharmaceutical manufacturers with a long history of success and now has an excellent opportunity for a good candidate to join the company. The Role Responsibility is to carry out all duties expected of a Qualified Person and ensure that product is manufactured in accordance with Good Manufacturing Practices. Experience The applicant will be eligible for appointment as a Qualified Person, have extensive experience of the pharmaceutical industry, GMP and will be degree qualified or equivalent. Keywords Pharmaceutical, Qualified Pers | |
| Development Formulation Scientist (Pharma) Our client is a highly successful, pharmaceutical manufacturing organisation based in West Lothian. Due to continued growth an excellent opportunity has now arisen for a Development/FormulationScientist to join their team. The role The key responsibility / core activity is to carry out formulation development involving new and existing active pharmaceutical ingredients to achieve specific release profiles (including Controlled Release). Other responsibilities include conducting compatibility/stability trials utilising specific techniques, such as coating, and generating internal and customer reports to a high standard. The candidate Successful candidates should have a qualification in Chemistry, Pharmacy or related field.Previous formulatio | |
| Head of Medical Information, Leading Healthcare Company - £50,000 SE Global Healthcare company seeks Head of Medical Information This is an unrivalled opportunity for a Head of Medical Information to join a global healthcare company located in the South East. The role of the Head of Medical Information is a critical role in today?s healthcare. This role will involve delivering the highest customer service standards in the industry through your team. The Head of Medical Information will be required to grasp a wide-ranging brief that includes: * Managing the department's budgets and business planning * Representing the company within the medical information community * Working with colleagues overseas to ensure globally consistent medical information. All applicants must have a life sciences degree and relevan | |
| Regulatory Affairs Officer // Thames Valley // £30 - £36K + Bens!!!! This company is a global pharmaceutical organisation based in Berkshire. The base of the European HQ, they are currently looking for a Regulatory Affairs Associate. As the successful candidate, you would be joining a team of 6 that are responsible for all the company?s projects and you would be expected to provide advice, support and regulatory documentation to the project you are currently assigned to. You will also be expected to ensure that clinical trials are conducted, both on and off site, as well as mentoring other members of staff within the team and assist with regulatory affairs training. To be successful in this role, you will be expected to demonstrate an excellent knowledge of GCP / GMP, global regulatory guidance and clinical | |
| Senior Medical Information Officer, Leading Pharma £40,000, South East Leading pharmaceutical company requires Senior Medical Information Officer ? 12 month fixed term contract This is an excellent opportunity for a Senior Medical Information Officer to join a leading pharmaceutical company in the South East. The role of the Senior Medical Information Officer is to provide a proactive, comprehensive, accurate and timely medical information service to internal and external customers. The role will require the Senior Medical Information Officer to: * Develop and maintain a thorough knowledge of the company?s products * Prepare and maintain all medical information reference documents, resource files and Q&As for allocated products * Provide specialist product medical input into submissions as required, e.g. NICE, | |
| Clinical Research Associate-Oncology-Biotech-SE -£30-32k Clinical Research Associate urgently required to join a successful Biotech in Cambridge. Financed by blue chip companies, this organisation has a broad pipeline of products in clinical and pre-clinical development. This biotech company is expanding it?s oncology team and is looking for an experienced CRA with Phase I oncology experience. This is an excellent opportunity to utilise your experience and bring your skills and oncology knowledge to the clinical team. You will be home based two days a week and based in the office for 3 days. Candidates must possess a life sciences degree and at least 1 years monitoring of phase I clinical trials. Contact Lizzy May at Real Pharmaceutical for more information on 0207 434 7966 or apply now! (Real IT | |
| Senior Clinical Project Manager, South East, £negotiable Senior Clinical Project Manager urgently needed to join a medium sized global CRO in the South East. Our client are looking for an experienced Senior Clinical Project Manager to Manage and oversee all aspects of a clinical research trial and act as the primary point of contact with the Sponsor. It will be your responsibility to Manage the Clinical Study Budget and monitor study progress to ensure all goals are achieved to set timeframes. You will have a strong educational background and the desire to progress to Executive level. In return of hard work, our client offer a competitive salary with a generous car allowance and benefits package. They offer extensive training and career development, however within this role you will need to hit t | |
| Clinical Project Manager-£35-40k-CRO-Oxfordshire Clinical Project Manager required to join the clinical team within this successful CRO. This organisation covers every aspect of clinical research, from Phase I studies to complete Phase IV programmes, working in different therapeutic areas and covering a broad portfolio of product types, including devices and vaccines. This organisation recruit experienced staff from different backgrounds including pharmaceutical, biotech, health and CRO. As Clinical Project Manager you will be responsible for overseeing the clinical team to co-ordinate the operational aspects of ongoing projects, and work to ensure the client's goals of time, cost, and quality performance are met. You will be responsible for assuring the quality and consistency of the com | |
| Clinical Project Manager-International CRO-Cambridgeshire-£30-40k Clinical Project Manager urgently needed to join a successful International CRO. This company assists at every stage of clinical development and registration of new pharmaceutical products and medical devices from Phase I (in their own clinics) to Phase IV. As Clinical Project Manager, you will be responsible for overseeing various clinical projects. You will be the initial contact for the UK and will also be liasing with other clinical teams across Europe. Candidates must possess at least 3-4years as a Clinical Project Manager within a CRO/Pharmaceutical environment. You will have excellent IT skills and effective communication to liase with CRA?s, Senior Project Managers and Programme Directors. This company work with a multitude of thera | |
| SCRA, World Pharma, >£32,000, South Senior Clinical Research Associate required to join a global pharmaceutical company in the South East. This pharmaceutical company specialises in diabetes, schizophrenia and osteoporosis amongst others. This organisation have just been reported to of had a very successful business quarter, gaining new projects and allowing growth within their clinical team. This position is ideal for someone that has had at least 1 year?s experience as a SCRA, or at least 3 years as a CRA and capable to take on more responsibility. Candidates will have a strong educational background with a minimum requirement of a BSc in life sciences. Contact Lizzy May at Real Pharmaceutical for a more detailed job description on 0207 434 7999 or apply to this role now! ( | |
| Clinical Research Associate, Italy, €45k +Benefits Global CRO seeks an experienced CRA to join their clinical team Milan, Italy. You will need to speak English well too. This organisation has recently acquired new projects and the position has arisen due to growth. You will be part of a world-renowned organisation and can progress to project management level or across departments quickly and easily should you desire to. Ideally you will have at least 3 years experience as a CRA, with a variety of therapeutic experience in a range of Phases. This company offer a competitive package including car allowance, bonus scheme and holiday! There is a great atmosphere in the clinical team and the company has a very high retention rate. Contact Lizzy May at Real Pharmaceutical for more information on | |
| Pre Clinical Project Manager, Scotland £neg Pre clinical project manager urgently needed to join a global CRO in Scotland. This role will involve you being responsible for overseeing clinical trials in Phases I + II. This is an excellent opportunity for an experienced Clinical Project Manager to gain pre clinical experience or to continue your career in Scotland. Candidates will ideally have a strong educational background with experience within a Pharma/CRO environment. This organisation has recently won new projects and are successfully expanding their clinical team. This is a great opportunity to gain experience within a medium sized CRO and to have the opportunity to add on new skills to your experience. This company offers strong training and development as well as excellent ben | |
| Clinical Research Manager, Scotland, £negotiable Clinical Research Manager required to join a Pharmaceutical company in Scotland. Our client is looking for an experienced Clinical Project Manager/Clinical Research Manager to help the development portfolio and support the commercialisation of marketed products. The salary of the role for Clinical Research Manager is negotiable and will be based on experience. The benefits of the package include company pension, holiday and car allowance. This role will involve you co-ordinating and managing clinical research projects on a regional level. You will provide clinical support to development and commercial projects so that project targets, budgets and timelines are met. As Clinical Research Manager it will be your responsibility to provide clini | |
| Senior Clinical Project Director, South East, £Neg Senior Clinical Project Director urgently needed to join a Global CRO based in the South East. This is an executive position and the salary is negotiable based on candidate?s experience. This organisation has a strong position in the CRO market and they are continually gaining new projects. Candidates must possess a strong history within the CRO environment, having worked at a senior director level previously. The ideal candidate will have an excellent educational background and a strong interest in all areas of clinical research. To find out more about the company and the responsibilities needed please call Lizzy May at Real Pharma on 0207 434 7999. Alternatively apply to this role now. Senior Clinical Project Director, South East, Clinica | |
| Head of Regulatory Affairs, Berkshire, £negotiable Head of Regulatory Affairs needed to join a CRO in Berkshire. You will be responsible in setting up the new regulatory department. Due to expansion, this CRO are looking to increase their regulatory presence in the UK by creating a new department. This CRO is a well renowned organisation with a broad range of clients. This is an ideal role for someone looking for a more challenging position helping to define and build a new team. Candidates will ideally have at least 6 years experience within Regulatory affairs. You will have a strong educational background and a strategic approach to your work. Contact Lizzy May at Real Pharmaceutical for more information on 0207 434 7999 or apply to this role now! (Real IT Resourcing Limited acts as an Em | |
| Clinical Project Manager, Netherlands, €100,000 Clinical Project Manager urgently needed to join a Global Pharmaceutical company in the Netherlands. Our client have a strong Oncology Pipeline and are looking for an experienced Clinical Project Manager to hit the ground running and oversee the clinical team for 6 months initially. Candidates will ideally have experience in Oncology trials, phase can be flexible. Those candidates that are Medical Doctors will have an advantage, however this is not essential. Candidates must be fluent in English and be available to relocate and/or start immediately. Contact Lizzy May at Real Pharma for more information on 0207 434 7999 or apply to this role now. Clinical Project Manager, Oncology, Netherlands (Real IT Resourcing Limited acts as an Employmen | |
| Clinical Project Manager, 6-9month fixed Contract, £neg A Clinical Project Manager is urgently needed to join a medium sized CRO in Yorkshire. It will be your responsibility to oversee the clinical team for a period of 6-9months. You will be responsible for arranging clinical trial logistics for a Respiratory trial. Candidates will be experienced Clinical Project Managers with a strong background from within a CRO/Pharma background. You will have a strong educational background and the ability to hit the ground running. Contact Lizzy May at Real Pharma for more information on 0207 434 7999 or apply to this role now. Alternatively email me at e.may at realresourcing.com A Clinical Project Manager is urgently needed to join a medium sized CRO in Yorkshire. CRO/Pharma background (Real IT Resourcing | |
| Clinical Project Manager, Manchester, >£45,000 Clinical Project Manager urgently needed to join a Global Pharmaceutical company in Manchester. You will be an experienced clinical project manager with at least 5 years experience in Clinical Research. You will have a strong educational background and the drive to take on a new challenge. This is an excellent opportunity to join an innovative Pharmaceutical company where you can oversee the clinical team and be responsible for CRA?s and organisation across teams. For more information, please contact me, Lizzy May at Real Pharmaceutical for more information on 0207 434 7999 or apply to this role now. (Real IT Resourcing Limited acts as an Employment Agency and an Employment Business) Benefits: Permanent Contact: Elizabeth MayRecruiter: Re | |
| Clinical Research Associate, Not for Profit Clinical Org. >£30,000 Clinical Research Associate urgently needed to join a Not for Profit Clinical Organisation in Central London. This organisation are looking for experienced Clinical Research Associates to monitor Phase I + II clinical trials in Oncology. This organisation offers a strong career development package whereby you can progress to project manager level or transfer your skills to a different department. This role is ideal for those candidates that are struggling with the commute out of London as it is in a very central location in the City. Candidates will have a strong educational background and clear passion for clinical research. Contact Lizzy May at Real Pharmaceutical for an informal chat about this role and others on 0207 434 7999 send your | |
| CLINICAL PROJECT MANAGER, YORKSHIRE >£45,000 Clinical Project Manager needed to join a global CRO In Yorkshire. This organisation has a large US presence and is developing their status in Europe quickly. This position has arisen due to growth as new projects are being acquired. Candidates will ideally have a science background and at least 7 years experience in Clinical Project Management. You will be responsible for effectively managing the activities of clinical studies and staff in a manner that ensures all timeframes and targets are met and that costs are under control. The basic salary is flexible on experience. You will also have a generous Car allowance, pension + bonus scheme in place. Contact Lizzy May at Real Pharmaceutical for more information on the company and flexibility | |
| Senior Clinical Project Manager, Buckinghamshire, £negotiable Senior Clinical Project Manager urgently needed to join a Global CRO in Buckinghamshire, in the South East of England. Our client requires an experienced Clinical Project Manager with experience of both hand?s on project managing as well as line management. Candidates will have a range of therapeutic and phase experience from within a CRO/Pharmaceutical Company. Candidates will have a strong educational background. The salary for the role is negotiable and dependent on candidate?s experience and capabilities. Contact Lizzy May at Real Pharmaceutical on 0207 434 7999 or apply to this role now. Senior Clinical Project Manager urgently needed to join a Global CRO in Buckinghamshire, in the South East of England. Senior Clinical Project Manager | |
| Clinical Project Manager, CRO, Cambridgeshire, c £30,000 Clinical Project Manager urgently needed to join a leading CRO in Cambridgeshire. You will act as the primary interface between technical, laboratory staff, Clients, Investigators and Data Managers. Strong communication skills will be essential, as you will be liasing with clients and investigators, attending meetings and protocol discussions, and helping to train other colleagues in the team. You will have gained enough experience to organise the clinical team effectively and have the ability and desire to learn new managerial skills and the capability to progress professionally within a successful and global Contract Research Organisation. Candidates must possess a BSc/Msc and at least 5 years experience within a Pharma/CRO environment as | |
| Clinical Data Manager ? Team Leader, South Yorkshire > £28000 One of Europe?s most notable clinical research organisations is currently looking for an experienced Clinical Data Manager, with the right attitude and background to lead a team of 3- 10 other clinical data managers. This is a hands-on position, so you?re CDM skills need to be sharp, and refined. Working on clinical databases, you will be involved in projects from the set-up stage, through to process, and finishing in database lock. Ideally, you will have three years experience in clinical data management from a pharmaceutical or CRO environment, and will have performed in this kind of role before. A BSc / BA is essential. This company are offering a stepping-stone opportunity. With frequent role, and salary reviews you can be fast-tracked | |
| Senior Clinical Research Associate, Yorkshire, >£35,000 Senior CRA urgently needed to join a Global Pharmaceutical Development company in Yorkshire. You will ideally have at least 3 years experience as a CRA within a Pharmaceutical/CRO environment. As Senior Clinical Research Associate you will be responsible for identifying, initiating and close out of investigational sites for clinical studies. You will have experience of writing clinical reports to ICH/GCP. Candidates will need to have at strong educational background and a strong desire to progress to Project Management level. This company has an exciting and strong pipeline and is expanding their team to fulfil the projects. Contact Lizzy May at Real Pharmaceutical or apply to this role now! (Real IT Resourcing Limited acts as an Employment | |
| Clinical Research associate-immediate-Global CRO-UK+Europe c£30,000 Clinical Research associate urgently needed to join a Global Contract Research Organisation. Your role will be to oversee study sites from initiation to close out. You must be able to join the clinical team with good working knowledge of CRA responsibilities, including monitoring trials and reporting their progress. Candidates will have at least 1 year?s experience as a CRA preferably within a CRO environment. You will have good knowledge of SOP?s, GCP/ICH and regulatory guidelines. This is an excellent opportunity to be part of a global organisation with possibilities to relocate and to travel. For those candidates, who are career driven and wish to succeed, the possibilities to progress to project manager status quickly are very real. You | |
| Senior Clinical Project Manager, CRO, France £Neg Home based Senior Clinical Project Manager?s urgently to join a Global CRO in France. This CRO has a global presence and a successful history of gaining innovative projects and trials. As Senior Clinical Project Manager you will be required to oversee the clinical team so that the clients expectations are managed to specified time frames and budgets. Candidates must possess at least 5 years clinical trial experience, having worked on International Clinical Trials. This is an excellent opportunity to continue your career within a global CRO but with the opportunity for a home based role. The salary is negotiable depending on experience. Contact Lizzy May at Real Pharmaceutical for a more detailed job description on 0207 434 7966 or apply to | |
| Senior Clinical Research Associate, Oxfordshire >£35k+Car Senior CRA urgently needed to join a full service CRO in Oxfordshire. This company offers a competitive basic salary, contributory pension and life insurance. As Senior Clinical Research Associate it will be your responsibility to manage 3rd party vendors including freelance monitors and CROs, Input into protocol and CRF design and Investigator and site selection. You will be required to initiate study set-up including ethics/regulatory submissions, negotiation of study budgets and timelines and initiation visits. Candidates will ideally have 2 years experience as a CRA having previously worked within a pharmaceutical, biotechnology or CRO. The ideal candidate will have previous experience managing 3rd party vendors. Candidates must have th | |
| Senior Clinical Research Associate * Int. CRO * SE - £27-29k Senior CRA urgently needed to join a successful Clinical Research Organisation in the South East. It is a comprehensive and successful Phase II?IV clinical services organisation looking for an experienced and determined senior clinical research associate. Your role will be to function as a Lead CRA, providing guidance to the project team so that monitoring activities are managed fully and reported accurately to Project Management. You will be responsible for clinical trial initiation and adhere to all applicable SOP?s and regulatory requirements. You will also be responsible for supporting new CRA?s. Candidates must possess a science related Bachelors degree and at least 4 years clinical monitoring experience. Strong communication skills ar | |
| Clinical Research Associate Office Based in Scotland-Biotech->£32,000 As clinical research associate for a global biotech, you will be a key member of the successful clinical team. This company?s main focus is oncology and you will therefore have a minimum of 2 years experience working in Phase I trials within this therapeutic area. Your role will be to cover the site selection, initiation, assessment and close out of sites. You will be responsible for recruiting investigators, initiating studies and monitoring the progress of investigator sites. Writing protocols and designing case record forms will be an important part of your day to day activities. Candidates will ideally have a strong educational background with a Life Science degree and the determination to progress to senior CRA status. Contact Lizzy Ma | |
| Dental Nurse Dental Nurse required for January 2009 start. To apply, please send your CV to michaela@mitrem.co.uk | |
| Community Nurse Manager An outstanding beacon of the local community, this healthcare trust provides specialist care to seriously ill people of all ages and backgrounds. Since the 1970s, the core services have included physical, psychological, social and spiritual care for patients and their relatives. An exceptional and inspirational Community Nurse Manager is required to join this leading healthcare provider. The successful candidate will be required to lead and coordinate the busy team of highly experienced and knowledgeable nursing specialists, working across the local community. You will be responsible for the care provision of over 1,500 patients and their families. The role is to ensure that the highest standards of individualised care are | |
| NVQ Assessor - Care Are you interested in training to become an NVQ Assessor? Are you in any of the following or related jobs? CARER, NURSERY NURSE, MANAGER, REGISTERED MANAGER, CARE ASSISTANT Our client is looking for competent people interested in undertaking training to be an NVQ assessor in the Hampshire area. Selected applicants would receive funding to complete the A1 Assessor qualification at no cost, with a view to securing employment in this growing sector in the future. Training can be undertaken flexibly to fit around current work commitments and on successful completion, New Futures Recruitment would assist you in finding an Assessors role either full or part-time. If you have sound practical and | |
| Pharmacy Technician Our client is currently searching for a Band 4 Pharmacy Technician, required to start ASAP and commit to at least 2-3 months. The duties will be based in Dispensary and previous Hospital experience is required. The Hospital is located within easy reach of British Rail, or a short bus ride from the Underground (Northern Line) **We are looking for technicians with NVQ 3 in Pharmacy Services, or equivalent, who are eligible to register with the Royal Pharmaceutical Society of Great Britain** All applicants should be flexible, have excellent communication skills and recent UK Hospital experience. In return, PULSE can offer: - Excellent rates of pay - Pulse Privilege - Employee benefit | |
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| Sales Specialist - Cardiology Equipment Sales Specialist - Cardiology Equipment UK Wide (home office) 40k Base, 50-60k OTE Car Bens Our client is a leading family owned manufacturer of medical devices, products and solutions used by medical staff at all levels around the globe. With over 100 years experience and a portfolio of products and solutions to meet with every need and budget they are well placed to deliver continuous growth on a global scale. They now have an exciting opening for a Sales Specialist to cover the UK form a home based office. As a Sales Specialist you will be responsible for developing both new and existing relationships throughout the UK with a focus on developing and achieving annual connectivity products sales targets. You | |
| Physiotherapist Band 7 Specialist Community Our client based in Blackpool is in need of a band 7 Locum Physiotherapist to start ASAP in their ongoing, full time position. The successful candidate will be required to work within their community team covering a caseload of rehab and neuro conditions with adult elderly patients. The candidate appointed needs to be confident at band 7 level as the majority of the time they will be working alone across the Blackpool area. Due to the nature of the work a car owner/driver is required. PULSE have been awarded Master Vendor contracts in North East London, South West London, North Central London and North West England . If you want first pick of work in these areas get in touch with us today! | |
| Physiotherapist Band 6 community Our client based in Surrey/South West London is in need of a band 6 locum Physiotherapist to start ASAP in an ongoing, full time or part time position. The successful candidate will be expected to work within Neuro or ICT with the Early Supported Discharge Team PULSE have been awarded Master Vendor contracts in North East London, South West London, North Central London and North West England . If you want first pick of work in these areas get in touch with us today! Due to the nature of the work a car owner/driver is required. Benefits of working for PULSE : Free annual Mandatory Training updates Free annual Occupational Health Clearances Holiday Pay Competitive | |
| Physiotherapist - Band 6 MSK O/P Our client based in North London is in need of a full time band 6 locum Physiotherapist to start 12th January for four weeks initially, full time hours. The successful candidate will be required to work within Musculoskeletal outpatients dealing with a PCT caseload. PULSE have been awarded Master Vendor contracts in North East London, South West London, North Central London and North West England . If you want first pick of work in these areas get in touch with us today! Benefits of working for PULSE : Free annual Mandatory Training updates Free annual Occupational Health Clearances Holiday Pay Competitive rates of pay An amazing selection of posts throughout the | |
| Pharmacist Our client is currently searching for a Band 6/7 Pharmacist, required to start ASAP and commit to at least 2-3 months. The duties are based in Dispensary/Wards, however the client will be willing to look at candidates with Hospital Dispensary backgrounds. Knowledge of the JAC system would be useful. All applicants should be flexible, have excellent communication skills and recent UK Hospital experience. In return, PULSE can offer: - Excellent rates of pay - Pulse Privilege - Employee benefit package** - Various employment opportunities in your preferred geographical area - Flexible hours to meet your needs, part or full time - Free Mandatory Training - Reimbursed Cri | |
| Dental Nurse A local, private dental practice is looking to recruit an experienced Dental Nurse to cover maternity leave. The main duties will be tidying and preparing the surgery, sterilising instruments, preparing materials, making sure the patient is relaxed and comfortable at all times , maintaining sterile conditions within the surgery, following health and safety guid | |
| Home Manager East Sussex Home Manager for Dementia Nursing Home in East Sussex, Hove - Nursing Home Manager for Elderly Dementia Home - Make a Fresh Start in January 2009!!! Excellent Role!!! Are you looking for a new challenge and a fresh start going into 2009 - have you been in a position for a while and you need something fresh to challenge and push you to the next step in your nursing home management career?? This could be the role for you. Eclypse Recruitment, Health & Social Care Recruitment Specialists are currently looking to recruit an experienced Home Manager. The home is part of a larger organisation who pride themselves on a being a successful business whilst running a caring and compassionate organisation. The elder | |
| Documentation Officer Our pharmaceutical client is looking to expand their team by taking on a Documentation Officer within the Quality Assurance (QA) Department. The position will help support a new project involving extensive GMP and Validation work being carried out at the site. The successful Documentation Officer will come from a Quality Assurance or QA background and will have extensive knowledge of GMP within a pharmaceutical manufacturing environment. Applicants must also be able to demonstrate an understanding of the control, design and monitoring of QA and validation documentation within a GMP environment. This position could be offered permanent or 2 yr temporary basis. For additional information please contact Richard Taylo | |
| Product Sales Specialist - Life Science Product Sales Specialist - Life Science Midlands and South Wales 28-38k Base, 38-50k OTE Car Exec Bens Our client is a global leader in Life Science and Technology using innovation and education to make a difference in everyday quality of life. Through their global workforce, this NASDAQ listed company delivers a growing portfolio of biochemical and organic chemical products and solutions to a growing range of sectors. Due to UK growth, they are now looking for a Product Sales Executive to cover parts of the Midlands and South Wales As a Product Sales Specialist you will manage a territory defined by postcode and be responsible for developing and implementing a business plan to manage activities, with particu | |
| Deputy Home Manager for Elderly EMI Nursing Home Deputy Home Manager for Elderly EMI Nursing Home - Must be a Qualified Mental Health Nurse with Supervisory Experience!!! £24-25k Taunton, Somerset!!! Excellent Opportunity! Eclypse Recruitment are specialists in Health & Social Care Recruitment. We are currently looking to recruit a senior Registered Mental Health Nurse with supervisory / management experience for an elderly EMI nursing home in Taunton, Somerset. The home is a 41 bedded Dementia & Alzheimers elderly nursing home. The home is situated within easy access of all local amenities and main bus routes / roads. It is a lovely home with a friendly and welcoming team; it is a purpose built home and is currently rated as good with CSCI. We are looking | |
| Senior Manager Regulatory Submissions A leading international biotech company is seeking a Senior Regulatory Submissions Manager to be based in their UK office. The main function of the role will be managing and preparing regulatory systems and documentation to facilitate project development and registration on an international level. You will liaise with regional submissions teams and provide support where needed to create and submit regulatory dossiers in accordance with appropriate legislation and timelines. You will take responsibility for streamlining the submissions process and providing dossier guidance to global cross-functional teams. You will have decision making authority for process improvement design and implementation, resource and submi | |
| Senior Quality Inspector Senior Quality Inspector An exciting opportunity has arisen for a Senior Quality Inspector within a well-established pharmaceutical company. The successful Senior Quality Inspector must have extensive knowledge in dealing with GMP in the pharmaceutical industry or have previously worked in a Senior Quality Inspector role. The Senior Quality Inspector will be responsible for quality inspections, in-process audits and the completion of quality documentation, batch records and COA. They will work closely with the QP gathering and recording all the information needed to allow the QP to sign off on batches. The successful Senior Quality Inspector will have good communication skills and excellent attention t | |
| Housekeeper/Companion Female* Housekeeper/Companion required. General duties to include laundry, housekeeping, shopping, preparing light meals, laundry and some assistance with laundry and some assistance with dressing/personal care. Are you an outgoing individual with lots of experience? Can you be diplomatic yet directive? Pulse Social Care are looking to employ an individual with the above skills. Hours required are approximately 2 per day initially, to be built upon as the relationship with the client develops. * SDA Section 7 (2)(B) applies. | |
| Spine & Trauma Sales Consultant Spine & Trauma Sales Specialists This is an excellent opportunity to specialise your career and move into the exciting field of medical device and theatre sales. The company is world class and is Internationally renowned with presence in over 50 countries. They are at the forefront of modern surgery and you will be promoting innovate products. As a theatre sales specialist you will be given huge responsibility in directing and training all theatre staff in using the company's portfolio of orthopaedic products. So an ability to work effectively under open surgery conditions is a must. You must be able to proactively refreshing your knowledge of surgery procedures and products. The ideal candidate will have NHS s | |
| Senior Safety Specialist - Belgium Senior Safety Specialist - Belgium Western Europe, ALL Second Post ?2000 - ?3500 per month + Excellent Banfits Senior Safety Specialist - Belgium Experienced Pharmacovigilance Officer required for a well established not for profit organisation based in Belgium. Fantastic package for the correct candidate. Job Description My client is seeking an enthusiastic, expereinced drug safety associate with sound knowledge of case processing and case management. My client is an academic organisation that seeks diversity in their employees and offers a fantastic package in return. You will: *Monitor all safety reports and alert the responsible Medical Officer of any discove | |
| Strategic Clinical Development Director, London: Research experience? An excellent opportunity has arisen for a strategically minded Clinical Director to join a highly progressive Pharmaceutical company based in a prime London location. This role is ideal for a senior level Clinical Research Scientist that is looking for a refreshing new small company environment. | As a strategic Clinical Development Director your main responsibility will be to take leadership and ownership in planning and implementing the projects to meet the company's corporate objectives. You will be proactive; working closely with Key Opinion Leaders (KOLs) and |
| Health Outcomes Manager Health Outcomes Manager ? Berkshirexml:namespace prefix = o ns = "urn:schemas-microsoft-com:office:office" /> £70K + Benefits Pharmacy Technician | |
| medical secretary This is an ACS vacancy who are operating as an employment agency. Medical Secretaries Required to work on a temporary on-going basis to start immediately.. Must have previous medical secretarial experience in an 'acurate' unit and able to deal with fast paced ward environment with busy clinics. Please email CV's to Eileen@acs-recruitment.co.uk | |
| Senior Regulatory Affairs Officer - Hungary Senior Regulatory Affairs Officer - Hungary Eastern Europe, ALL Junior Management ?30000 - ?50000 per annum My client, a leading clinical research organisation, are looking for an Senior Regulatory Authorisation Associate to be based in their office in Hungary. You can expect to work for an organisation who are dedicated to the people they have working for them by offering good career progression, a relaxed atmosphere and advancement opportunities. Your main duties will be to prepare EC submission packages according to the relevant requirements for selected countries and collect and update information on EC and regulatory requirements in selected countries. You must have relevant | |
| Regulatory Affairs Manager - Sweden Regulatory Affairs Manager - Sweden ALL Senior Management ?40000 - ?60000 per annum My client, a leading clinical research organisation, are looking for a Regulatory Manager to be base their office in Sweden as part of a new and growing team. You can expect to work for an organisation who are dedicated to the people they have working for them by offering good career progression, a relaxed atmosphere and advancement opportunities. You will be responsible for maintaining a clear overview of regulatory developments, monitoring, identifying and implementing new regulatory strategies and requirements and providing expert regulatory input into new business proposals and bid defense meetings. | |
| SAS Programmer SAS Programmer Western Europe, ALL Second Post £40000 - £55000 per annum + Benefits My client a leading CRO based near Geneva require a SAS programmer to join their European Head Office function. The ideal candidate will have 12 months professional experience within the Pharmaceutical industry doing SAS Programming. This role will also involve some statistical work and eventually become a Biostatistician so would suit someone looking to make their first steps at getting experience as a Biostatistican. The role will entail the points below plus any other ideas your able to bring to the table from past experiences gained. *Receive, load, verify structure of external data *Development an | |
| Dug Safety Associate Dug Safety Associate Western Europe, ALL Second Post £3000 - £40000 per annum + Benefits Job Summary: A Pharmacovigilance officer is required for an expanding Drug Safety Specialist Consultancy in the Switzerland. Excellent opportunity for a Drug Safety associate looking for promotion. Market leading remuneration package and an excellent opportunity for an interesting and varied work load. Requirements: Job Description. My client is a forward thinking consultancy company and is currently seeking an enthusiastic drug safety associate for their expanding Pharmacovigilance team. This role is ideal for a junior level associate looking for progression and development. Main Du | |
| Regulatory Affairs Manager - Clinical Trials - Netherlands Regulatory Affairs Manager - Clinical Trials - Netherlands Western Europe, ALL Middle Management £35000 - £50000 per annum Clinical Trial Submissions Manager - Exciting Opportunity in Clinical Research Join one of the industry's most experienced and specialised clinical trial management teams. My client - a global contract research organisation, manages the clinical trial process for pharmaceutical companies. You can expect to work independently within an international team in a continuously growing company, individual development opportunities and a competitive compensation package. The European activities are growing rapidly, and my client is currently seeking the following positio | |
| Regulatory Affairs Director - Switzerland Regulatory Affairs Director - Switzerland Western Europe, ALL Senior Management £100000 - £101000 per annum My client, a leading pharmaceutical company in Switzerland (Basel) is looking for a Global Program Regulatory Director (GPRD) for their General Medicines department. You can expect to work for a company committed to retaining and motivating associates through continued career advancement, be rewarded for dedication and achievement and encouragement to focus on achievement through collaboration and innovation. You will be the global regulatory affairs leader of a global program/brand team consisting of at least one key project in development or a brand with major ongoing development activi | |
| Part-Time Regulatory Affairs Senior Manager - Drug RA - Onc Part-Time Regulatory Affairs Senior Manager - Drug RA - Onc South East, England, UK, ALL Senior Management £25000 - £26000 per annum My client, a leading pharmaceutical company, seeks a Part-time Senior DRA Manager for their Clinical Development & Medical Affairs department for 3 days a week (flexible). As an employee - an associate - you will become part of an exciting global team dedicated to healthcare. Not only is my client committed to attracting the best but they also encourage long term professional and personal growth through their development programmes. You can expect to work for an international organisation and this means that there are many upwards and lateral development opportu | |
| Regulatory Affairs Manager Regulatory Affairs Manager Western Europe, ALL Junior Management ?50000 - ?60000 per annum My client, a successful, leading manufacturer of homeopathic combination medicines, is looking for an experienced and forward thinking regulatory affairs project leader to join the team in Germany. You can expect to work for a committed company who are represented in more than 50 countries, whose goal-oriented employees stand behind every product and guarantee the success of modern homeopathy. You will have good, solid experience in regulatory affairs and ideally be a medical practitioner, vet or pharmacist. I can also consider applications from people with a biological sciences background. English and | |
| Regulatory Affairs Officer - Netherlands Regulatory Affairs Officer - Netherlands Western Europe, ALL Second Post ?30000 - ?40000 per annum My client, a leading clinical research organisation, are looking for a Regulatory Affairs Associate to be based in their office in Netherlands. You can expect to work in a culture which is professional but friendly, fast paced but relaxed, challenging but highly rewarding, but also fun! My client is one of a small group of organisations with the capability and expertise to conduct clinical trials on a global basis. If you are keen to expand your career internationally, they will work hard to give you all the support and encouragement you need to develop your career in any global location. This is a cont | |
| Commercial Director Our Client, an Independent communications agency has an opportunity for a Commercial Director to lead the commercial team and new business development activities, and actively contribute to all aspects of the organizations corporate strategy. | |
| Pharmacy Technician Our client is looking for a Band 4 Pharmacy Technician, to start immediately for a duration of 3 months initially. Full time position, 37.5 hour/week. Duties include Dispensary and ward top up. We are looking for technicians with NVQ 3 in Pharmacy Services, or equivalent, who are eligible to register with the Royal Pharmaceutical Society of Great Britain. This Hospital is centrally located. Easily accessible by public transport or car, ample parking is available. Affordable accommodation is available on site. All applicants should be flexible, have excellent communication skills and recent UK Hospital experience. In return, PULSE can offer: - Excellent rates of pay - Pulse Priv | |
| Physiotherapist Band 5 graduate Our client based in Bolton is in need of a Band 5 graduate to start ASAP for one - three months initially, full time. The successful candidate is required to work within their wards on a rotational bases covering areas such as elderly, medical, orthopaedics, surgical etc. http://www.pulsejobs.com/uk/allied-health/ PULSE are currently running a new recommend a friend scheme. For every candidate that you recommend that works for over 200 hours we will pay you £150! After 6 months, if you have recommended 5 people that we have got out wo |