Teams at Parexel

Supports clinical and scientific conduct of clinical studies, including adjudication, medical monitoring, imaging data reconciliation, meeting materials, protocol deviation management, and study data review. The role may support multiple studies, interact with study sites and committees, and lead limited-scope studies. Responsibilities also include resolving data discrepancies, reviewing patient and medical record information, maintaining compliance with ICH-GCP and company processes, and completing required administrative tasks.

Manages clinical trial sites throughout study phases, serving as the primary site contact. Conducts remote and on-site monitoring, verifies data quality and participant safety, manages regulatory documentation, supports site activation and closeout, resolves compliance and performance issues, and maintains trial systems. Collaborates with investigators, sponsors, and cross-functional teams while supporting audits, inspections, mentoring, and study deliverables. Requires extensive domestic and international travel.

Conducts qualification, initiation, monitoring, and termination visits for clinical trial sites. Manages site quality, performance, regulatory documentation, data integrity, investigational product accountability, enrollment support, and compliance with protocols, Good Clinical Practice, SOPs, and regulations. Serves as the primary contact for investigators and site teams, resolving issues and safeguarding participant safety across oncology, ophthalmology, metabolic, hematology, or CAR-T studies.