Offer summary
Qualifications:
Bachelor's Degree in Life Science or related field preferred, 1-3 years of CRC or CTC experience, Knowledge of eTMF and ICH GCP.Key responsabilities:
- Support project team with administrative tasks and audit readiness
- Coordinate trial activities, review documents, resolve findings
- Communicate risks, analyze study metrics, maintain documentation
- Facilitate site start-up, update systems, support regulatory submissions