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Consultant Medical Writer
Ividata Life SciencesConsultant rédacteur médical chez IVidata Life Sciences à Paris. Rédaction de documents cliniques réglementaires et collaboration avec des experts en santé.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
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 ExperienceRegulatory Requirements KnowledgeCollaboration with Clinical TeamsQuality Control of DocumentsFluent in English
ATS Keywords
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Hard Skills
Medical WritingRegulatory Document DraftingScientific MonitoringQuality ControlClinical Documentation
Soft Skills
AutonomousRigorousLeadership
Certifications & Qualifications
Master's DegreePhD
Industry Keywords
Pharmaceutical IndustryConsultancyRegulatory Affairs
About the role
Key responsibilities & impact- 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
What you’ll need- 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)
Benefits
Comp & perks- Stimulating environment at the heart of health innovation
- Remote work option