Northeast, remote with travel as needed
Position Overview
The Director will lead clinical pharmacology strategy and execution across multiple development programs, providing scientific expertise, data-driven insights, and cross-functional leadership. This role requires strong analytical, strategic, and communication skills to interpret clinical data, shape development plans, and influence decision-making within a matrixed R&D environment.
Key Responsibilities
- Design and lead clinical pharmacology studies, from protocol to final report
- Serve as study lead and contribute to clinical development and translational plans
- Interpret PK/PD data and contribute to regulatory documents (e.g., INDs, NDAs)
- Collaborate with internal teams to resolve program challenges and guide strategy
- Represent clinical pharmacology in regulatory interactions and cross-functional meetings
Essential Qualifications
- Ph.D., M.D., or Pharm.D. with 5+ years in clinical pharmacology within the pharmaceutical industry
- Strong knowledge of PK/PD, modeling tools, and regulatory frameworks
- Oncology, pediatric, or translational medicine experience preferred
- Excellent communication and cross-functional leadership skills
