Analista Sr Start-up Estudos Clinicos

Coordinate and execute the import and shipment activities of clinical supplies for all studies under responsibility, ensuring compliance with applicable requirements. Review import documentation for Investigational Product (IP) and other materials, ensuring completeness before shipment. Maintain accurate records related to import and shipment activities, ensuring traceability and readiness for audits.

Bachelor's degree in health or scientific area or equivalent. 1-2 years of experience in clinical research, preferably with 1 year or more in Study Start-Up in the designated region. Practical knowledge of ICH guidelines and GCP.