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Director, Global Medical Information & Scientific Communications (Biotech)

200 000 - 250 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
director
Английский
b2
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

Director, Global Medical Information & Scientific Communications (Biotech): Lead execution of comprehensive medical information and scientific communications strategy across pipeline assets for allogeneic CAR-T therapies with an accent on operational excellence, compliant scientific exchange, and global trial site support. Focus on developing MI processes and content, MC deliverables, publications planning, and engaging external stakeholders like investigators and KOLs.

Location: Remote based in the U.S. (must be authorized to work in the U.S.; up to 40% travel including international)

Salary: $200,000–$250,000 per year

Company

Clinical-stage biotechnology company pioneering allogeneic CAR T cell (AlloCAR T™) therapies for cancer and autoimmune diseases.

What you will do

  • Lead Medical Information support for pipeline assets, including SOPs for inquiry handling, response development, and maintaining content library (SRLs, FAQs).
  • Drive Medical Communications in partnership with stakeholders and vendors, developing scientific platforms and deliverables like slide decks and congress materials.
  • Lead publications planning and execution per GPP and ICMJE standards, coordinating review committees and supporting abstracts, posters, and manuscripts.
  • Engage external stakeholders (investigators, KOLs, societies) for publications and trial site support.
  • Provide site support for ALPHA3 global trial sites, including SIV attendance and investigator meetings.
  • Ensure compliance with regulations, policies, and MLR requirements across activities.

Requirements

  • Advanced degree in life sciences (PhD, PharmD, MD, APN)
  • 4-6+ years in Medical Affairs (Medical Information, Communications, Publications) in pharma/biotech; pipeline/launch experience preferred
  • Understanding of medical affairs, scientific content lifecycle, HCP relationships, and scientific exchange
  • Authorized to work in the U.S.; ability to travel internationally (~40% time)
  • Excellent communication, presentation, time management, and organizational skills
  • Familiarity with legal, regulatory, compliance for scientific exchange across geographies

Culture & Benefits

  • Fast-paced, dynamic, collaborative biotech environment
  • Competitive compensation with annual bonus and equity
  • Health insurance, generous time off including 2 company-wide holiday shutdowns
  • Opportunity to work with experienced cell therapy team on innovative therapies

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