Offer summary
Qualifications:
College/University Degree in Life Sciences, Administrative work experience in international settings, Prior experience as CTA for CROs, Prior experience in Clinical Research, Full working proficiency in English and Spanish.
Key responsabilities:
- Act as main contact for site personnel and CRA, resolving queries
- Manage regulatory submissions, ensuring compliance with local regulations
- Assist Monitors with subject and site event information in CTMS
- Coordinate audits, inspections, and TMF management
- Track clinical supplies order and inventory management