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Sr. Clinical Development Medical Director
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- Establishes and approves scientific methods for design and implementation of clinical protocols, data collection systems and final reports.
- Essential Duties and Responsibilities: Design, prepare, and initiate study protocols and other required documentation in compliance with project plans, federal regulations, GCP, and good medical practice.
- Collaborate with internal safety group in analyzing and reporting of safety data from clinical trials.
- EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: MD (board certification or eligibility in Oncology or Hematology/Oncology desirable but not essential) required with a minimum of 8 years of post-residency experience.
- Equivalent combination of education and experience Experience/The Ideal for Successful Entry into Job: Drug development experience in biotechnology or pharmaceutical industry, or a combination of academia and industry.
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