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Senior Director, Oncology Pharmacology

232 000 - 348 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior/director
Английский
b2
Страна
US/Ireland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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

hirify.global 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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