1 день назад
Senior Director, Oncology Pharmacology
232 000 - 348 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Director, Oncology Pharmacology (Oncology Drug Development): Leading oncology pharmacology teams and programs from discovery through regulatory approval with an accent on immuno-oncology, complex therapeutic modalities, and translational preclinical research. Focus on designing efficacy and biomarker studies, managing CRO and academic collaborations, integrating preclinical and clinical datasets, and authoring nonclinical regulatory submissions.
Location: Remote/Home-Based for US-based candidates in California, Palo Alto, CA, or Philadelphia, PA
Salary: $232,000–$348,000 USD base pay, plus potential bonus, equity, and benefits.
Company
is a global biopharmaceutical company developing medicines for serious diseases, with a growing portfolio of oncology treatments and research programs.
What you will do
- Lead oncology pharmacology scientists and serve as a pharmacology lead for one or more programs from discovery through regulatory approval.
- Design and execute studies assessing efficacy, tolerability, mechanisms of action, pharmacodynamics, and biomarkers in hematologic malignancies and solid tumors.
- Evaluate therapeutic combinations and modalities including small molecules, biologics, ADCs, bispecifics, cell therapies, gene therapies, and RNA-based therapeutics.
- Manage CRO and academic research collaborations, including protocols, timelines, budgets, study execution, and data interpretation.
- Collaborate with Clinical Development, Bioanalytical, Toxicology, Clinical Pharmacology, Biomarkers, Regulatory Affairs, and Project Management teams.
- Prepare technical reports and contribute to IND, NDA/BLA/MAA, briefing package, DSUR, IB, and fast-track designation documentation.
Requirements
- Ph.D. in biology, biochemistry, immunology, pharmacology, or a related discipline.
- Extensive industry experience in oncology drug development, from hit-to-lead optimization through IND-enabling studies.
- Deep immuno-oncology expertise, including in vivo and in vitro models, immune cell biology, and immunological endpoints.
- Experience across multiple therapeutic modalities and with cancer signaling pathways.
- Proven leadership of complex pharmacology programs across CROs, including GLP and non-GLP studies.
- Direct people management, strong project management, analytical skills, and experience authoring nonclinical regulatory submissions.
Culture & Benefits
- Remote/home-based work arrangement for the specified US locations.
- Highly matrixed, cross-functional collaboration across internal teams, academia, industry, CROs, and regulatory agencies.
- Medical, dental, and vision insurance.
- 401(k) retirement savings plan and flexible paid vacation.
- Potential annual cash bonus or incentive compensation and discretionary equity grants.
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