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6 часов назад

Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline

182 000 - 346 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior/director
Английский
c1
Страна
US
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
Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline (Oncology/Medical Affairs): Leading medical and scientific strategy for AbbVie's global prostate cancer oncology pipeline with an accent on evidence generation, clinical research, scientific communications, and patient safety. Focus on designing development strategies and protocols, engaging medical experts, coordinating cross-functional stakeholders, and translating clinical data into global medical affairs plans.

Location: Mettawa, Illinois; Florham Park, New Jersey; or South San Francisco, California, United States. Hybrid schedule with office attendance Tuesday through Thursday.

Salary: USD 182,000–346,000 annually, plus eligible benefits and long-term incentive programs.

Company

hirify.global develops medicines and healthcare solutions in areas including immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead medical input into disease-area and asset strategies for the prostate cancer oncology pipeline.
  • Lead medical evidence-generation strategies, including company-sponsored studies, research collaborations, and investigator-initiated studies.
  • Provide scientific expertise and coordinate medical activities with clinical development, commercial, regulatory, discovery, statistics, and market access stakeholders.
  • Develop medical expert engagement strategies and gather insights from internal and external stakeholders.
  • Lead scientific narratives, congress planning, medical education, publication strategies, and communications.
  • Support clinical research activities, regulatory discussions, safety surveillance, risk minimization, budgets, timelines, and compliance.

Requirements

  • Scientific Director: PhD or PharmD, typically 10–15 years of pharmaceutical industry or equivalent experience, including 7–10 years in Medical Affairs.
  • Senior Medical Director: M.D., D.O., or equivalent medical degree, with at least 2 years of clinical trial or medical affairs experience.
  • Substantial knowledge of the relevant therapeutic area; direct prostate cancer experience is strongly preferred.
  • Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements, development strategy, and protocol design.
  • Proven leadership in cross-functional global teams and the ability to support global business strategy.
  • Excellent written and spoken English communication skills are required.

Culture & Benefits

  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility to participate in long-term incentive programs.
  • Work across global medical affairs, clinical, commercial, regulatory, and research functions.

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