2 дня назад
Medical Content Development Manager / Team Lead (Medical Information)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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