Offer summary
Qualifications:
Bachelor's or advanced degree in science, Fluent in local language and English, Excellent understanding of clinical research, Hands-on knowledge of Good Documentation Practices, Good IT skills and adaptability.Key responsabilities:
- Ensure compliance of study conduct
- Manage clinical research sites and visits
- Communicate with site staff on protocol issues
- Identify and resolve performance problems
- Mentor junior CRAs and lead audit activities