Jobs at Parexel

Lead country-level study operations from startup through close, overseeing local teams, vendors (pCRO/CTM/SCP), timelines, budgets, risks, and compliance. Provide operational input, manage site activation and recruitment strategies, ensure TMF completeness, support new technologies (eConsent, eISF, remote SDV/SDR, iConnect), and liaise with global stakeholders to resolve escalations and optimize study delivery.

Lead and oversee global clinical study start-up activities and CRO partners to drive site activation, timelines, and compliance. Develop and approve start-up plans, coordinate regional stakeholders, solve operational challenges, and ensure regulatory and GCP adherence across assigned programs.

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.