Study Physician - Cambridge

C.K. Associates Limited
£750 to £950
27 Sep 2017
03 Nov 2017
Contract Type
Full Time
Farzaana Khan is recruiting for a GMC registered physician to join as a Study Physician in Oncology for a specialist pharmaceutical company at their site based in Cambridge on a contract basis with opportunity to work from home. The main purpose of the role will be to: - Manage global or regional studies within the Immuno-Oncology franchise and will be involved in the design, conduct, monitoring, data interpretation and reporting of individual clinical trials, ensuring that all clinical studies operate to the highest ethical and safety standards and in compliance with Good Clinical Practice (GCP) and regulatory requirements. - Will have a strong clinical and specialty background in Oncology and/or Immuno-Oncology and will be a peer among the industry, medicine and/or academic community within the field of pharmaceutical medicine and/or area of Immuno-Oncology specialty. - Will provide expert scientific and clinical input to teams in the Immuno-Oncology therapeutic area under the direction of the Global Clinical Lead (GCL) - Serve as a trial level physician and medical monitor for clinical studies. Have responsibility for protecting the integrity and conduct of clinical studies. Provide consultation to clinical operation colleagues on protocol design questions and answering protocol related questions from site investigators. In order to be considered for this role, you will be required to have the following qualifications and experience: - Graduate of a recognized school of medicine with an M.D. degree or equivalent. - Board Certification or Eligibility in Oncology is required; specialty training and/or clinical experience and strong academic track record in Immuno-Oncology, Tumour Immunology, or Immunotherapy is preferred. - Three (3) or more years of direct industry drug development experience or 3-4 years' post fellowship clinical trial experience in an academic setting collaborating with pharmaceutical sponsors. - Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including an understanding of biostatistics and safety reporting. - Ability to conduct a large study as part of a global team. - Ability to function within a matrix environment; to contribute to decision-making and reaching alignment in order to meet challenging timelines. Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained. CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL40211 in all correspondence.
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