Jobs at Parexel

Manages clinical trial investigator sites from activation through close-out, ensuring patient safety, GCP compliance, protocol adherence, data quality, and timely study execution. Responsibilities include onsite and remote monitoring, site relationship management, investigator and staff training, recruitment support, adverse event follow-up, investigational product oversight, issue resolution, CAPA remediation, documentation, audit support, and database release activities. Requires extensive clinical research monitoring experience and frequent travel.

Lead and coordinate clinical trial site activation and operational activities from start-up through close-out. Manage Investigator Initiation Packages, essential documents, regulatory and ethics submissions, site issues, compliance tracking systems, and collaboration with regulatory and supporting teams. Ensure activities meet study timelines, applicable laws, Good Clinical Practice, sponsor standards, and local requirements.

Leads Parexel’s commercial strategy to drive new business growth, market positioning, and high-value bid pursuits. Responsibilities include market and competitive analysis, bid triage, sales messaging, RFI/RFP strategy, client presentations, cross-functional stakeholder alignment, win-loss analysis, industry engagement, and commercial effectiveness initiatives. The role requires executive-level client relationship management, CRO industry expertise, strategic influence, and leadership of global teams.

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.