Job Summary The SrCRA role is responsible for supporting monitoring and site management activities for the client Sponsored studies. Site monitoring and site management activities are conducted according to ICH GCP, applicable country/local regulations and client SOPs. Site interactions are conducted both on-site and off-site with documented interactions recorded in CTMS.

The role involves collaboration with cross-functional clinical study teams and investigator site personnel to ensure study deliverables are met efficiently and effectively. The SrCRA is also responsible for the oversight of activities carried out at investigator sites where the monitoring may be supported by a CRO partner through the review of operational data and metrics. Key Responsibilities

Site Management and Monitoring Activities Perform site management activities to ensure compliance with the protocol, monitoring plan, ICH GCP, local regulatory requirements, and client SOPs. Conduct site qualification, initiation, interim, and close-out visits, both on-site and remotely. Partner with Clinical Trial Liaison (CTL) and other client functions (e.g., Study Start-Up, Global Partnerships and Trial Optimization) to support site activation and deliverables.

Establish and maintain productive professional relationships with investigator site staff, ensuring effective communication and problem-solving throughout study conduct. Perform drug accountability, reconciliation, and destruction, ensuring protocol compliance for storage and shipment requirements.

Oversight Monitoring

Prepare and maintain Oversight Monitoring Plan. Perform review of study metrics, assess CRO Clinical Research Associate (CRA) and Investigator Site performance and identify sites for oversight monitoring visits.

Conduct Oversight Monitoring

Visits at sites, either independently or alongside CRO CRA. Review site source documentation and verify accurate data capture (ALCOA principles). Review and report on status of stud