Offer summary
Qualifications:
Bachelor's Degree in Life Science preferred, 1-3 years of CRC or CTC experience, Excellent business communication skills, Knowledge of eTMF and ICH GCP, Proficient in MS Office and clinical trial databases.
Key responsabilities:
- Provide administrative and technical support for project teams
- Coordinate activities for assigned trials and ensure compliance with protocols
- Perform document reviews and maintain accurate system records
- Assist with site activation and stakeholder communication
- Train new personnel and contribute to global strategic processes