Teams at Parexel

Lead site selection, initiation, monitoring (onsite and remote), and close-out activities for oncology clinical trials. Ensure ICH‑GCP, local regulations, and sponsor SOP compliance; manage regulatory submissions, drug accountability, data quality, safety reporting, eTMF/CTMS updates, and readiness for audits/inspections while supporting site performance and risk‑based monitoring.

The Clinical Operations Manager oversees trial protocols, manages budgets, ensures compliance with regulations, coordinates teams, and collaborates with vendors for clinical operations.

Monitor clinical sites through qualification, initiation, monitoring and close-out visits. Build site relationships, ensure patient safety and regulatory/GCP compliance, verify data quality and drug accountability, manage regulatory documentation, and support recruitment strategies to meet enrollment timelines.