Role OverviewThe Senior Principal Scientist has primary responsibility for planning and directing clinical research activities involving new or marketed Oncology medicines. The Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.
What You Will Do
Evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications; Developing of clinical development strategies for investigational or marketed Oncology drugs; Planning clinical trials (design, operational plans, settings) based on these clinical development strategies.
Why It Might Be a Fit
The Senior Director may supervise the activities of Clinical Scientists in the execution of clinical studies; work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Senior/Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.
Requirements
- M.D or M.D./Ph.D.
- Minimum of 3 years of clinical medicine experience.
- Minimum of 3 year of industry experience in drug development or biomedical research experience in academia.
- Demonstrated record of scientific scholarship and achievement.
- A proven track record in clinical medicine and background in biomedical research is essential.
- Strong interpersonal skills, as well as the ability to function in a team environment are essential.
- Outstanding verbal and written communication and presentation skills.
Benefits
- Medical, dental, vision healthcare and other insurance benefits (for employee and family)
- Retirement benefits, including 401(k)
- Paid holidays, vacation, and compassionate and sick days
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