Associate Director Clinical Pharmacology
About The Position
The Associate Director in the Clinical Pharmacology group provides strategic and scientific expertise and represents Clinical Pharmacology at relevant meetings. The role provides subject-matter support to new and ongoing clinical programs, primarily in oncology. It proactively identifies and delivers significant clinical pharmacology contributions to research and development programs, including complex work that addresses strategic program needs, advances program science, or resolves regulatory hurdles. The role contributes to overall program development and communicates complex strategies and results to development teams in an influential manner. The Associate Director independently designs and conducts, or oversees the development of, analysis plans and applies standardized or advanced scientific techniques for pharmacokinetic, pharmacodynamic, and other quantitative analyses. The role timely informs management of results and issues and prepares accurate, well-articulated clinical study reports and regulatory submission documents. It calls for advanced clinical pharmacology knowledge, scientific leadership, mentorship, and the ability to influence change and contribute to multidisciplinary and cross-functional teams. The position is based in Tarrytown, New York; Warren, New Jersey; or Cambridge, Massachusetts, with a work model requiring four days per week onsite.
Requirements
- PhD in Biology, Pharmacology, Engineering, Pharmacy (Pharm.D.), or Medicine (MD).
- At least 8 years of relevant Clinical Pharmacology experience.
Responsibilities
- Identify and provide significant clinical pharmacology contributions to research and development programs, including complex work addressing strategic program needs, scientific advancements, or regulatory hurdles.
- Contribute to strategic program development and communicate complex strategies and results influentially to development teams.
- Independently design and conduct, or oversee the development of, analysis plans.
- Apply standardized or advanced scientific techniques to conduct pharmacokinetic, pharmacodynamic, and other quantitative analyses.
- Inform management of results and issues in a timely manner.
- Prepare and deliver accurate, well-articulated clinical study reports and regulatory submission documents on time.
- Represent Clinical Pharmacology at relevant meetings and contribute scientific expertise to multidisciplinary meetings.
- Provide mentorship and clinical pharmacology subject-matter support to new and ongoing clinical programs, primarily in oncology.
- Influence and effect change within the organization and with external groups, and collaborate with cross-functional teams.
Benefits
- Competitive and comprehensive total rewards package, which may include annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, medical, dental, vision, life and disability insurance, paid time off, and family support benefits.
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What This Job Offers
Job Type
Full-time
Career Level
Director
Education Level
Ph.D. or professional degree
