Medical Writer

📍 Location: Remote
✈️ Travel: Minimal (occasional team meetings and scientific conferences)

About the Role

As a Medical Writer, you will be responsible for developing high-quality clinical study documentation to support the company's medical products across a range of pre-market and post-market studies. Working closely with cross-functional teams, you'll play a key role in generating clinical evidence that supports both regulatory requirements and improved patient outcomes.

Key Responsibilities

• Author clinical study protocols, clinical study reports, and other clinical investigation documentation.
• Prepare clinical data summaries for internal stakeholders, healthcare professionals, patients, and regulatory authorities.
• Ensure all documentation is developed in accordance with Good Clinical Practice (GCP).
• Conduct literature reviews and database searches (PubMed, Embase) to support study design and evidence generation.
• Collaborate with global teams across multiple business units.

About You

• BSc with 3-5 years of relevant experience, or MSc/PhD with 1-2 years of relevant experience.
• Proven experience writing clinical study documents, particularly protocols and clinical study reports.
• Trained in Good Clinical Practice (GCP).
• Excellent scientific and written communication skills.
• Strong literature review and evidence assessment capabilities.
• Experience with CTMS and eTMF systems is advantageous.
• Knowledge of the medical device and/or pharmaceutical industry is preferred.