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2 дня назад

Medical Content Development Manager / Team Lead (Medical Information)

Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
lead
Английский
c1
Страна
UK/Europe/Italy
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 Content Development Manager / Team Lead (Medical Information): Developing scientifically rigorous medical information and medical communications content for pharmaceutical, biopharmaceutical, medical device, and digital therapeutic products with an accent on evidence-based writing, MLR review, and client delivery. Focus on managing document development, fact checking complex scientific data, coordinating medical writers, and maintaining compliant, high-quality content.

Location: Home office based, with the role listed in Milan, Italy. Eligible candidates must hold a valid work permit in the European Union or the UK. Business travel of approximately 10–15% may be required.

Company

hirify.global provides commercialization services and medical solutions for life sciences companies, supporting pharmaceutical, biotech, medical device, and digital therapeutic products.

What you will do

  • Develop scientific and medical content, including scientific response documents, FAQs, slide sets, abstracts, posters, and education materials.
  • Manage the full document development process, from gathering source materials through medical, legal, and regulatory review.
  • Own content in document management platforms such as Veeva PromoMats and MedComms, including reference anchoring and annotations.
  • Perform scientific data fact checking and collaborate with medical reviewers, medical writers, creative teams, and clients.
  • Provide direction to medical writers and contribute to project strategy, client meetings, SOPs, templates, and process improvements.

Requirements

  • At least two years of experience in the pharmaceutical industry or with a medical information or medical communications service provider.
  • Master’s or doctoral degree in life sciences, healthcare, or an equivalent field.
  • Experience developing global medical information materials such as SRDs, FAQs, and custom response documents.
  • Strong scientific writing, editing, presentation, project management, and client communication skills.
  • Experience with literature searches using PubMed, Ovid, or Embase and reference management tools such as EndNote, Mendeley, or Citavi.
  • Valid work permit in the European Union or the UK is required.

Nice to have

  • Pharm.D., Pharm.M., medical degree, PhD, or relevant bachelor’s degree in life sciences.
  • Experience across multiple therapeutic areas and with product launches and ongoing medical content management.
  • One or more additional European languages at B2, C1, or C2 level.

Culture & Benefits

  • Full-time home-office position with flexible scheduling based on client and management needs.
  • Collaborative work across global medical information, medical affairs, medical writing, and creative teams.
  • Focus on patient interests, client outcomes, ethical standards, diversity, inclusion, and continuous improvement.
  • Opportunities to evaluate and implement new technologies and procedures that improve efficiency and content quality.

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