Consultant Medical Writer

• Work on high-value projects as a Medical Writer
• Draft and review regulatory clinical documents
• Collaborate with Clinical, Regulatory and Medical Affairs teams
• Perform quality control of complex documents
• Contribute to scientific monitoring and writing processes

Requirements

• Master's degree or higher in a scientific field (Physician, Pharmacist, Scientific Master’s degree or PhD)
• Minimum of 5 years' proven experience in medical writing within the pharmaceutical industry or a consultancy
• In-depth knowledge of regulatory requirements (EU and US)
• Autonomous, rigorous and demonstrates leadership
• Fluent in English (spoken and written)

Core Competencies

Demonstrates expertise in drafting and reviewing regulatory clinical documents, with a strong understanding of EU and US regulatory requirements. Proven ability to collaborate effectively with Clinical, Regulatory, and Medical Affairs teams while ensuring high-quality standards in medical writing.

Highest-signal resume keywords

• Medical Writing Experience
• Regulatory Requirements Knowledge
• Collaboration with Clinical Teams
• Quality Control of Documents
• Fluent in English

ATS Optimization Keywords

Hard Skills

• Medical Writing
• Regulatory Document Drafting
• Scientific Monitoring
• Quality Control
• Clinical Documentation

Soft Skills

• Autonomous
• Rigorous
• Leadership

Certifications & Qualifications

• Master's Degree
• PhD

Industry Keywords

• Pharmaceutical Industry
• Consultancy
• Regulatory Affairs