Teams at Parexel

Monitors and manages clinical trial sites from qualification through closeout, ensuring protocol, GCP, regulatory, data, safety, documentation, and investigational product compliance. Conducts site visits, trains investigators, reviews source data and essential documents, tracks action items, maintains CTMS records, supports audits and study teams, and collaborates with sites and functional groups. Requires substantial travel and Phase I monitoring experience.

Leads clinical trial site activation from feasibility through initiation, managing critical paths, regulatory and ethics requirements, documentation, timelines, risks, systems, and cross-functional teams. Serves as a client-facing subject matter expert, guides activation staff, oversees quality and compliance, analyzes metrics, improves processes, and supports proposals and business development across multiple studies and therapeutic areas.

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.