Teams at Parexel

Manages clinical trial sites throughout study phases, serving as the primary site contact and conducting remote and on-site monitoring. Ensures compliance with protocols, ICH-GCP, regulations, and sponsor procedures while protecting participant safety and data quality. Oversees site documentation, recruitment, performance, issue resolution, and audit readiness. Collaborates with internal teams, vendors, investigators, regulators, and ethics committees. Mentors junior CRAs, supports inspections, contributes to process improvements, and travels domestically and internationally approximately 65%–75% of the time.

Lead global clinical trial projects for mid-to-large biotech and pharmaceutical clients. Manage project teams, daily operations, schedules, resources, budgets, and cross-functional coordination while ensuring timely, high-quality delivery and regulatory readiness. The role requires clinical development expertise, strategic problem-solving, strong organization, and client-facing leadership across the full clinical trial process.

Leads clinical data management activities across study startup, conduct, and closeout. Manages delivery timelines, database milestones, data integrations, risks, quality, compliance, audits, resources, and sponsor requirements. Collaborates with global cross-functional teams, supports proposals and financial management, maintains inspection-ready documentation, and provides training and mentorship. Requires extensive clinical data management experience and expertise with Medidata Rave and related clinical trial systems.