What are the responsibilities and job description for the Medical directors of Oncology Clinical Research – San Francisco position at TANNER & ASSOC INC?
Medical Directors of Oncology Clinical Research – San Francisco
Tanner and Associates is recruiting several Medical Directors of Oncology Clinical Research for large Biotech companies located in San Francisco, Los Angeles, Salt Lake, and New Jersey. Candidates can be based out of any of these locations.
Do not wait to apply after reading this description a high application volume is expected for this opportunity.
Requirements :
Several major Biotech companies are seeking Medical Directors / Clinical Scientists with drug development experience to join the Oncology program. Candidates should have an M.D. with board certification / eligibility in hematology / oncology, or a PhD, PharmD with at least 5 years of drug development experience. Prior experience in clinical trials in an oncology-related field is preferred. Candidates must be comfortable proactively solving issues and working independently.
Job Duties and Responsibilities :
The role primarily focuses on the design, implementation, analysis, and interpretation of clinical trials from phase I-III. The candidate will be expected to contribute significantly to the strategic direction of the Oncology programs, including clinical trial design, implementation, analysis, interpretation, and dissemination of results. Additionally, the candidate will be required to build and maintain excellent relationships with outside parties, including clinical investigators, advisors, regulatory authorities, and collaborating companies.
Responsibilities : Design :
- Design clinical experiments, including drafting protocol summaries and providing clinical input to complete protocols.
- Provide initial clinical designs for future trials, partnering with research, translational oncology, biostatistics, clinical operations, regulatory, and pharmacology for input / alignment and presentation at the Therapeutic Development Team meetings.
- Serve as a key member on the Clinical SubTeam, providing significant input into the clinical development / strategy.
Implementation :
Analysis and Interpretation :
J-18808-Ljbffr
