Назад
Company hidden
обновлено 1 день назад

PharmD Program Associate - Regulatory Strategy (Biotech)

98 100 - 160 100$
Формат работы
onsite
Тип работы
fulltime
Грейд
trainee
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
PharmD Program Associate - Regulatory Strategy (Biotech): Supporting global regulatory planning and execution for pharmaceutical products across clinical development, approval, and lifecycle management with an accent on regulatory pathways, submissions, safety data, and cross-functional delivery. Focus on drafting regulatory documents, analyzing clinical and safety data, managing vendors and timelines, and preparing strategies for interactions with global health authorities.

Location: Onsite in Tarrytown, New York, United States. Travel of up to 15% may be required. Applicants must be eligible to work permanently in the United States.

Salary: $98,100–$160,100 annually.

Company

Biotechnology organization developing pharmaceutical products through global clinical development, regulatory, and safety programs.

What you will do

  • Support global regulatory planning and execution for clinical development, product approvals, and lifecycle management.
  • Develop regulatory strategies and define pathways in collaboration with cross-functional partners.
  • Draft documents for clinical sites and regulatory submissions.
  • Analyze clinical-study and safety data for interactions with ethics committees, management, and regulatory authorities.
  • Manage third-party vendors and maintain timelines for key results and deliverables.
  • Participate in a 24-month rotational program with mentorship and optional exposure to another functional area.

Requirements

  • PharmD graduate from an accredited ACPE College of Pharmacy, or a PhD in a related life-science discipline.
  • PharmD and/or PhD degree must be completed by Summer 2027.
  • Familiarity with evaluating clinical trials, scientific literature, and clinical data.
  • Permanent U.S. work eligibility is required.
  • Strong motivation to build a career in clinical sciences, global clinical operations, regulatory affairs, or safety sciences.

Nice to have

  • Prior internship or rotational experience in the pharmaceutical or biotechnology industry.

Culture & Benefits

  • Structured 24-month interdisciplinary development program with training from experienced mentors.
  • Cross-functional assignments and hands-on experience across global development areas.
  • Opportunities to travel to clinical sites and meetings with health authorities.
  • Comprehensive rewards may include bonuses, equity, retirement benefits, health and wellness programs, insurance, paid time off, and family support benefits.
  • Inclusive workplace with reasonable accommodations available during recruitment where required.

Hiring process

  • Submit a resume and cover letter specifying the preferred program track; rank multiple tracks if applicable.
  • Applications are accepted from August 24 through September 11, 2026.
  • The interview process is described in the program brochure.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →