We recruit across the full drug development process for a large number of the worlds leading clinical research organisations from pre-clinical through Phase I, Phase II, Phase III and Phase IV. We work with niche early phase through to global late phase and full service CROs with responsibility for product development, formulation and manufacturing; clinical trial management, clinical, medical and safety monitoring; preclinical, toxicology, and clinical laboratory services for processing trial samples; data management, biostatistics and medical writing services for preparation of an FDA or EMEA submissions
Clinical Research Associates (CRAs) are vital for the conduct of clinical trials. We manage CRA vacancies for the clinical research, pharmaceutical and biotechnology sectors to ensure compliance with clinical trial protocols, checking clinical site activities, making on-site visits, reviewing Case Report Forms (CRFs) and communicating with clinical research investigators. Whether you are a field based CRA or office based CRA, you will be a key part of monitoring clinical trials
Flame Pharma recruits experienced clinical project management and clinical operations professionals to provide clinical management of successful clinical trials. Clinical Management Professionals have responsibility for client liaison, clinical trial design and set-up, plus responsibility for managing the trial successfully and to budget. If you are involved in the pharmaceutical sector providing clinical management throughout the whole trial or have the variety of managing a number of trials within a CRO, then Flame Pharma provides clinical management opportunities for the worlds leading organisations from Phase I-Phase IV
Flame Pharma works with a number of the world’s leading Pharmaceutical Companies. With the pharmaceutical industry developing, producing, and marketing drugs licensed for use as medications, (either in generic and/or brand medications) they are subject to a variety of laws and regulations regarding the patenting, testing and marketing of drugs. Flame Pharma recruits for all pharmaceutical professionals from drug discovery through drug development to market.
We specialise in supplying Regulatory Affairs professionals to the pharmaceutical, clinical research, biotechnology and medical device sectors. With strict regulations in the drug development process, we recruit leading regulatory professionals to ensure that their companies comply with all of the regulations pertaining to their business. Our regulatory affairs professionals advise their companies on the regulatory aspects and climate that would affect proposed activities, working with local regulatory agencies and international agencies such as the Food and Drug Administration (FDA) or European Medicines Agency (EMEA).
We recruit Medical Writing professionals for pharmaceutical, clinical research, biotechnology and medical communications/medical writing agencies. Whether you are a medical writer in the pharmaceutical/CRO sector (preparing documents for submission to the regulatory authorities and manuscripts for publication, plus writing projects such as training manuals, promotional material for marketing purposes and websites) or a potentially more creative opportunity as medical writer in a medical communication agency (preparing manuscripts for publication, items for conferences e.g. posters, abstracts, and slide presentations, promotional items for pharmaceutical marketing, training material, and multimedia e.g. websites), we provide medical writing expertise throughout the UK and Europe
We specialise in providing Medical Advisors, Medical Directors, Research Physicians and Medical Affairs Managers for all Medical Affairs positions, being responsible for a full range of medical and clinical requirements with leading pharmaceutical, clinical research and biotechnology companies. If you are looking for a Medical Affairs role writing clinical product development plans for key therapeutic areas, or responsibility for medical affairs strategy on a global scale, or having patient responsibility as a research physician, then contact Flame Pharma
We specialise in recruiting pharmacovigilance and drug safety professionals responsible for the successful planning, forecasting and management of global resources for the completion of client projects for Global Drug Safety, plus overall responsibility for the planning, co-ordination and delivery of a variety of research projects through teams of safety specialists. With responsibility for identifying new information about hazards associated with medicines and preventing harm to patients, Flame Pharma represents some of the most exciting roles in Pharmacovigilance and Drug Safety for some of the world’s leading pharmaceutical, clinical research and biotechnology companies
Flame Pharma recruits experienced research nurses and nurses from the NHS to help run successful clinical trials. Clinical Research Nurses have responsibility for input into trial paperwork and data collection throughout a trial (helping administer drug formulations, taking bloods and recording observations) and having responsibility for patient and volunteer welfare. This is a fantastic career path for NMC registered nurses either from the NHS or Clinical Research/Pharmaceutical looking to become involved in the development of tomorrows medicines
Flame Pharma recruits experienced research physicians and doctors from the NHS to help run successful clinical trials. Clinical Research Physicians have responsibility for input into trial paperwork and data collection throughout a trial (helping administer drug formulations, recording observations and liaising with clients on events from the trial) and having overall responsibility for patient and volunteer welfare. This is a fantastic career path for GMC registered doctors/physicians either from the NHS or Clinical Research/Pharmaceutical looking to become involved in the development of tomorrows medicines
We recruit for a number of pharmaceutical, clinical research and biotechnology companies in their analytical services departments. As drug formulations need to have strict testing, the analytical scientist analyse samples using appropriate methods, (such as HPLC, GC, and LC) to the required standards producing high quality data. More experienced analysts develop and validate analytical methods, and ensures that equipment/instrumentation is calibrated and maintained and that laboratory records/documentation comply with cGMP’s. The analytical scientist’s role is highly technical using some of the industries most sophisticated equipment and techniques such as HPLC, GC-MS, ELISA and SDS-Page. Whether you are an analytical scientist working for a pharmaceutical or an analytical services company, we provide the best possible career options for analytical scientists
Flame Pharma provides recruitment solutions within Clinical Business Development and Sales for the Pharmaceutical and Clinical Research Sectors. High profile Business Development Directors and Managers within pre-clinical, drug safety, central laboratory services, early phase, bioanalytics, and clinical services are represented through our global network. We also represent medical, pharmaceutical, hospital and equipment sales professionals providing expert sales solutions to the world’s leading pharmaceutical, clinical and medical device companies
Pharmaceutical, Clinical Research and Biotechnology companies require all clinical data to be quality checked for accuracy and integrity. Quality assurance (QA) professionals provide the systematic and independent examination of all trial-related activities and documents. These audits determine whether the evaluated activities were appropriately conducted and that the data were generated, recorded, analysed, and accurately reported according to protocol, standard operating procedures (SOPs), and good clinical practices (GCPs). We recruit for all levels and areas of Quality Assurance professionals, from QA Executive to Quality Auditor, Director of Quality Management Systems and Qualified Person (QP).
Flame Pharma works alongside leading Biotechnology and Biopharmaceutical companies involved in ground breaking research in areas such as genetics, microbiology, animal cell culture, molecular biology, biochemistry, embryology, and cell biology). Other areas of expertise also include chemical engineering, bioprocess engineering, and information technology. We recruit across the full Biotechnology industry, recruiting specialist scientists researching into new biological molecules ( proteins) and targetting the underlying mechanisms and pathways of diseases and illnesses. We recruit across all disciplines within these research areas including regulatory affairs, research and development, process engineering and manufacturing, coupled with providing some of the world’s leading scientists to the Biotechnology and Biopharmaceutical sector.
We work with leading clinical research, pharmaceutical and biotechnology companies in recruiting their full data management staffing requirements. We recruit staff from the initial stages of clinical data collection and management using clinical data management systems and eCRFs. We recruit data managers to oversee the clinical the data management process to ensure all data is screened for typographical errors, and data can be validated to check for logical errors prior to being analysed and sent to the regulatory authorities for approval. We also manage vacancies for SAS Programmers, Programmer Analysts, Biostatistician and Statisticians across all levels to Senior Management and Director.
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Medical Affairs - Clinical Research Physician
Assistant Regulatory Affairs Manager In West
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