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Medical Reviewer, CRF Design
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Medical Reviewer, CRF Design – Ref NJ 13448
This is an excellent opportunity for a GMC registered physician to work for a leading global CRO that provides a comprehensive range of services in Phase I-IV clinical trials to the pharmaceutical, biotechnology and device industries. They are seeking a doctor with the relevant experience in clinical trials including clinical protocols and CRF development to join their Medical Affairs department in Eastleigh, Hampshire.
JOB ROLE: The Medical Reviewer contributes to the CRF design process, with focus on ensuring the scientific, medical and operational completeness of the CRFs / eCRFs
PRINCIPAL RESPONSIBILITIES include:
• Liaising with sponsors and project teams to ensure complete and accurate information is provided to the CRF design team to allow production of complete CRFs/eCRFs.
• Providing expert opinion on the content of CRFs/eCRFs and ensuring the final CRF/eCRF is fit for purpose for the capture of all required data, in particular the primary and secondary analysis variables.
• Identifying any risks or limitations to final CRFs/eCRFs and ensuring these are adequately discussed with the sponsor.
• Participating in the review of the draft CRF/eCRF to ensure they are complete, accurate and meet all requirements of client and the sponsor.
• Understanding a protocol and providing feedback to the project team / CRF design group on design issues, with regards to the protocol requirements.
• Working with other members of the project team. This includes the Project Manager, Sponsor, Programmer, Statistician, CRA and Data Manager.
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
• Medical degree with GMC Registration
• Relevant experience of the clinical protocol / CRF development process desirable
• Thorough understanding of clinical trial processes
PERSONAL SKILLS & ATTRIBUTES:
• Excellent written and oral communication skills
• Attentiveness and accuracy to detail
• Effective organisational skills
• The ability to manage workload on several parallel projects
BENEFITS OF THE ROLE: This Company has been nominated as a “top CRO” on 20 out of 25 site relationship attributes by pharmaceutical media company Thomson CenterWatch. They have an outstanding track record with a style of work that has been rated as the highest in the in the industry. They believe that their staff are their most vital asset and are committed to providing all the assistance and support you require to enable you to reach your goals and develop your career as far as you want it to go. Salaries are competitive and they offer an excellent benefits package including financial and long service awards.
Fforde is a uniquely specialised recruitment agency/business for the pharmaceutical, clinical research and biotechnology sectors with a glowing reputation in the industry. For applications please email your CV to: stella@fforde-management.com or speak to our specialist consultant, Stella Daniel who will be pleased to give you further information and advise on your personal career needs. Tel: +44 (0)1273 222957
Visit our website at www.fforde-management.com
KEY WORDS: Medical Reviewer, CRF Design, Medical Degree, MD, GMC Registered, Clinical Protocol, CRF Development, Clinical Research, Clinical Trials, CRO
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