Medical (Scientific) Writer

Join our Regulatory Affairs department as a Medical (Scientific) Writer. Position is in any EU country .

Medical (Scientific) Writer is responsible for the preparation of various documents used in clinical research and marketing authorization of medicinal products.

Role responsibilities:

• Prepare documents for marketing authorization of medicinal products (CTD modules 2.4, 2.5, 4, 5) and clinical research across all phases (study protocols and reports, Informed Consent Forms, Investigator’s Brochures, etc.), including writing, QC, resolving reviewers comments
• Write manuscripts for scientific journals
• Research on topics relevant to assigned projects
• Communicate and co-operate with other team members and clients
• Contribution to process improvements

• Master or higher degree in Medicine, Pharmacy, Public Health or Life Sciences
• Fluent written and spoken English...