**European Senior Medical Writer ** 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.

Must have skills and Qualification****s:

• 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.