Medical Directors of Oncology Clinical Research Los Angeles
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.
Interested in learning more about this job Scroll down and find out what skills, experience and educational qualifications are needed.
Requirements :
Major Biotech companies are seeking Medical Director / Clinical Scientist with drug development experience to join the Oncology program.
The candidate 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 responsibilities are primarily focused 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 external parties, including clinical investigators, advisors, regulatory authorities, and collaborating companies.
Responsibilities : Design :
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.
- Serve as a key member on the Clinical SubTeam, providing significant input into clinical development / strategy.
Implementation :
- As Medical Monitor, be responsible for all aspects of certain key clinical trials as per ICH / GCP guidelines.
- Partner with Data Management for CRF, tables, listings, figures design, and data quality plan.
- Medical monitoring of Phase I-III trials, serving as the primary Clinical Science contact on the Protocol Execution Teams and the primary liaison for clinical operations.
- Perform regular clinical reviews of listings and partner with clinical operations / drug safety to develop a safety monitoring plan.
Analysis and Interpretation :
- Analyze interim and final data, including interpretation and representation / explanation of results in verbal and written format.
- Possess excellent technical understanding of oncology.
- Have a strong understanding of the clinical trial process, particularly the role of the Medical Monitor, including compliance requirements.
- Demonstrate excellent written and verbal communication skills.
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