Teams at Syneos Health

Conducts clinical trial site qualification, initiation, monitoring, management, and close-out activities while ensuring GCP, regulatory, protocol, patient safety, and data integrity compliance. Reviews source documents, clinical data, investigational product records, and trial files; resolves queries; supports recruitment, audits, training, site communication, and project timelines. May support real-world late-phase studies through chart abstraction, regulatory coordination, site identification, and process improvement. Requires regular travel of up to 75%.

Manages country-level clinical trial site start-up activities, including regulatory and ethics submissions, essential document collection, site activation, milestone tracking, budget monitoring, and TMF filing. Provides country regulatory intelligence, supports site feasibility and selection, coordinates investigators and functional teams, and may assist with contract and budget negotiations. Ensures compliance with SOPs, work instructions, timelines, quality standards, and applicable local regulations.

Supports country-level clinical trial site start-up activities, including regulatory and ethics committee submissions, essential document collection, site activation, milestone tracking, budget monitoring, vendor coordination, and Trial Master File maintenance. Provides country regulatory intelligence, assists with investigator contracts and budgets, supports site feasibility and selection, and facilitates communication among investigational sites, project managers, and functional teams while ensuring compliance with SOPs, ICH GCP, and local regulations.