About the job
Become a vital part of our Regulatory Affairs team as a Medical (Scientific) Writer. This position is open to candidates located in any EU country.
The Medical (Scientific) Writer plays a crucial role in developing a variety of documents essential for clinical research and the marketing authorization of medicinal products.
Key Responsibilities:
- Draft and refine documents for the marketing authorization of medicinal products (CTD modules 2.4, 2.5, 4, 5) and clinical research, including study protocols and reports, Informed Consent Forms, Investigator’s Brochures, and more. This includes writing, quality control, and addressing reviewer feedback.
- Create manuscripts for publication in scientific journals.
- Conduct thorough research on topics pertinent to assigned projects.
- Foster effective communication and collaboration with team members and clients.
- Contribute to process enhancements and improvements.

