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19 часов назад

Associate Director, Medical Reviewer (Pharma Review)

115 900 - 322 900$
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
Associate Director, Medical Reviewer (Pharma Review): Providing final medical and scientific approval for promotional and non-promotional pharmaceutical and medical device materials for US clients with an accent on FDA, PhRMA, FTC, and medical review compliance. Focus on critically analyzing research evidence, resolving complex review issues, advising cross-functional teams, and leading training and reviewer development.

Location: Home-based in the United States; occasional onsite visits to clients may be required

Salary: $115,900–$322,900 annualized base pay

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Lead medical content review committees as the final approver for promotional and non-promotional pharmaceutical and medical device materials.
  • Approve client assets in line with strategy, standard operating procedures, and applicable regulations.
  • Provide expert guidance on FDA, PhRMA, and FTC requirements, approval processes, and review best practices.
  • Collaborate with Commercial, Regulatory, and Legal partners and serve as an escalation point for complex reviews.
  • Represent Medical Affairs in client meetings, business development discussions, and proposal requests.
  • Support training, reviewer recruitment and onboarding, coaching, audits, and expansion of the US market.

Requirements

  • Advanced science or medical degree such as PharmD, PhD, or MD, or equivalent experience.
  • At least 3–5 years of direct US promotional or medical review experience, with the ability to work independently.
  • Ability to critically analyze research design, methods, and outcome measures.
  • Advanced knowledge of pharmaceutical and medical device guidelines and regulations.
  • Experience with an approval system such as Veeva Promomats or Aprimo is desirable.

Culture & Benefits

  • Remote, home-based work arrangement in the United States.
  • Potential onsite client visits as required by the role.
  • Health, welfare, and other benefits may be available.
  • Incentive plans, bonuses, or other compensation may apply depending on the position.
  • Equal opportunity employment with a focus on integrity and compliance.

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