About the role
Work Mode: Remote (Global Welcome)
Experience: 5+ Years
Target Markets: Portugal, Netherlands, Switzerland, Sweden, Denmark, Poland, Greece
Role Overview:
We are looking for experienced European Senior Medical Writers to support product launch activities across key European markets. This role requires strong expertise in localized medical communication, with a deep understanding of regional language nuances, healthcare systems, and regulatory environments. The ideal candidate can translate complex scientific data into market-relevant, culturally aligned, and compliant content for HCPs and patients.
Key responsibilities:
- Develop, review, and adapt medical content for European markets (Portugal, Netherlands, Switzerland, Sweden, Denmark, Poland, Greece).
- Support product launch communication including pre-launch, launch, and post-launch assets.
- Create and localize content across formats (visual aids, slide decks, emailers, websites, brochures, patient materials, video scripts).
- Ensure content aligns with local language, cultural context, and market expectations. Interpret and summarize clinical and scientific data into clear narratives.
- Collaborate with cross-functional teams (medical, strategy, creative, digital).
- Ensure scientific accuracy and compliance with regional regulations.
- Participate in client discussions and provide market-specific insights.
- Qualifications: Master's degree or higher in Life Sciences, Medicine, Pharmacy, or related field with 5+ years experience in medical writing/communications.
- Expertise in local market nuances (at least 1–2 of the listed target countries).
- Proficiency in English and local European language(s) preferred: Portuguese, Dutch, German, French, Swedish, Danish, Polish, Greek.
- Experience in content localization and adaptation for HCPs, patients, and consumers.
- Experience in branded and non-branded pharma communication.
- Familiarity with omni channel assets.
- Strong scientific writing and storytelling skills.
- Client-facing communication experience.
Nice-to-have:
- Experience with EU regulatory guidelines (EMA, local codes).
- Exposure to multilingual content workflows (e.g., Veeva).
- Experience working with regional affiliates.