Teams at Parexel

Collect clinical data and specimens per protocols and ICH-GCP; perform physiological measurements, phlebotomy, and assist with invasive procedures; operate clinical equipment; maintain CRFs and documentation; participate in quality control, audits, and risk mitigation in an early phase onsite unit.

The role involves designing clinical development programs, conducting statistical analyses, and ensuring evidence aligns with global strategies for Access and HTA needs.

Conduct site monitoring visits, manage site relationships, ensure compliance with protocols, and evaluate trial data integrity in clinical research.