Description
You will be the Leader of cross-functional teams, liaising with discovery, regulatory, clinical and commercial colleagues. Input to regulatory documentation, external relationship management (key opinion leaders) and review of literature pertaining to the product under development.- Integrate the research and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of clinical research professionals, or by supporting such a team as an expert in one or more areas of clinical research.
- Ensure there is adequate input into the drug development process from experts in each of the various areas of drug development, or provide input into one or more of these areas as a technical expert.
- Ensure own work, and work of team, is compliant with Safety, Health and Environment standards and all other relevant internal and external regulations.
Experience / Qualifications:
- Master's degree in a scientific field is required; considerable relevant experience in the pharmaceutical industry is preferred, however academic experience will be considered provided the candidate has current immune-therapy / oncology clinical trials experience.
- Phase II/III industry-sponsored clinical trials experience is required; late stage (e.g., Phase IIIb/IV) would be a plus.
- Experience managing and interpreting the results of clinical trials as well as exposure to writing protocols to some degree.
- Ability to work collaboratively in a cross functional setting.
- Well developed communication skills.
Experience leading and managing a team and project management experience is desirable