About this role
Role Overview
- primary responsibility for planning and directing clinical research activities
- managing the entire cycle of clinical development including study design, placement, monitoring, analysis, regulatory reporting, and publication
- evaluating pre-clinical and translational work to generate early clinical development plan
- developing clinical development strategies for investigational or marketed Oncology drugs
- planning clinical trials and monitoring the conduct of ongoing or new clinical trials
- analyzing and summarizing clinical findings to support decisions regarding safety and efficacy
- supervising activities of Clinical Scientists
- collaborating with a cross-functional group of experts
Requirements
- M.D or M.D./Ph.D
- Must have experience in industry or academia
- Demonstrated record of scientific scholarship and achievement
- A proven track record in clinical medicine and background in biomedical research
- Strong interpersonal skills
- Ability to function in a team environment
Benefits
- medical, dental, vision healthcare and other insurance benefits (for employee and family)
- retirement benefits, including 401(k)
- paid holidays
- vacation
- compassionate and sick days