Teams at Syneos Health

Conducts clinical trial site qualification, initiation, monitoring, management, and close-out visits while ensuring protocol, regulatory, and GCP compliance. Reviews source documents, medical records, informed consent, clinical data, investigational product handling, and essential trial files. Supports recruitment, audit readiness, query resolution, site training, documentation, and project timelines. May mentor junior CRAs and support real-world late-phase studies through chart abstraction, regulatory coordination, site identification, and sponsor collaboration.

The CRA II- SCRA conducts site qualification and management activities, ensuring compliance with regulatory guidelines, supporting patient recruitment, and documenting site activities.

The CRA II- SCRA will oversee site activities, ensuring compliance with regulatory standards while performing monitoring, data verification, and site management throughout the study lifecycle.