Offer summary
Qualifications:
Must have a medical degree, 4-6 years of related experience, Strong understanding of drug development and ICH, Familiarity with Good Clinical Practices, Strong written and verbal communication skills.
Key responsabilities:
- Provide medical guidance and oversight on studies
- Support clinical safety and project management
- Review data sets and critical study materials
- Participate in protocol development and training sessions
- Document contacts per study-specific procedures