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Clinical development
June 27, 2019

Clinical Program Director - Oncology

Your mission
  • Collect scientific data, interact with research stakeholders and provide medical and scientific expertise on the therapeutic areas and products of your scope;

  • Elaborate and propose clinical development plans and define the design of clinical studies of this plan; monitor the progress of the studies and analyze the results;

  • Participate as a scientific referent in pre-IND meetings, Scientific Advices and other interactions with authorities (EMA, FDA, and other local authorities);

  • Collaborate in the drafting or review of the main documents of the studies; collaborate in the CPC writing and its submission, including interactions with the registration authorities;

  • Propose positioning strategies and medical expertise to the Marketing teams for life cycle management and pre-launch products;

  • Provide support and interface with clinical operations and other internal and subcontracted clinical development stakeholders.

Expected profile
  • Physician with at least 3 years' experience in the pharmaceutical industry in clinical development or medical affairs;
  • Ideally, an oncologist by training or with a first experience in oncology ;
  • You have experience in submitting to the MA and interacting with authorities;
  • You are autonomous and organized;
  • You have a good level of English, both written and spoken.
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