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13 часов назад

Medical Information Manager (Biotech)

Формат работы
hybrid
Тип работы
fulltime
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
Medical Information Manager (Biotech): Developing and maintaining scientifically balanced medical information materials, standard responses, educational resources, and product dossiers with an accent on medical communications, literature research, and product lifecycle support. Focus on responding to healthcare professional inquiries, identifying and escalating adverse events and product complaints, and managing documentation in Veeva MedInquiry.

Location: Hybrid role based in the RTP, NC office, requiring at least three days per week onsite; in-office requirements may increase based on business needs.

Company

hirify.global is a publicly traded biotech and pharmaceutical company developing therapies for rare diseases and technologies that expand the availability of transplantable organs.

What you will do

  • Develop and maintain standard response documents, FAQs, AMCP dossiers, slide decks, leave-behind materials, and other medical affairs resources across the brand lifecycle.
  • Research and prepare scientifically balanced responses to unsolicited on-label and off-label medical information requests.
  • Translate scientific literature and clinical trial data into educational materials for healthcare professionals and internal audiences.
  • Manage medical information requests and escalations in Veeva MedInquiry, supporting timely and accurate responses.
  • Identify and report adverse events and product complaints to Global Patient Safety in accordance with SOPs and compliance requirements.
  • Support scientific congress activities, publications and clinical trial resources, insights forums, and medical affairs initiatives.

Requirements

  • Doctor of Pharmacy (PharmD) degree with an active pharmacy license.
  • At least two years of pharmaceutical industry medical information or hospital experience.
  • Experience searching Embase and PubMed, abstracting databases, and retrieving full-text literature.
  • Knowledge of Medical Information and Medical Affairs regulations and guidelines.
  • Ability to manage multiple projects, collaborate cross-functionally, and communicate clearly in writing and verbally.
  • Proficiency in Microsoft Word, PowerPoint, Excel, and databases.

Nice to have

  • Medical writing experience or a Medical Information Fellowship.
  • Experience developing field medical slides for external use.
  • Experience with IRMS or Veeva Medical Information systems.
  • Clinical experience in pulmonary hypertension.
  • Participation in an accredited medical writing association.

Culture & Benefits

  • Mission-driven environment focused on unmet medical needs and rare diseases.
  • Eligible employees may receive medical, dental, vision, and prescription coverage.
  • Benefits may include wellness resources, 401(k), ESPP, paid time off, paid parental leave, and disability coverage.
  • Work is performed in a collaborative, cross-functional medical affairs environment.

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