Offer summary
Qualifications:
5+ years experience in medical or scientific writing, Ability to interpret and present complex data, Excellent written communication skills and attention to detail, Organizational skills and ability to work on multiple projects, Knowledge of drug development and regulatory environment.
Key responsabilities:
- Prepare clinical regulatory documents such as protocols and CSRs
- Lead project teams in producing high-quality, accurate documents
- Work closely with cross-functional teams for efficient document development
- Ensure deliverables meet all regulatory guidelines and internal standards
- Assist in designing templates and maintaining standards for clinical documents