The CRA is responsible for the initiation, monitoring and closure of assigned sites in clinical studies, in compliance with sponsor's procedural documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies. Frontline liaison between the sponsor and sites to ensure successful collaboration.

Monitor clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported per protocol. Coordinate activities to set up and monitor a study. Senior CRAs manage trials and support Project Managers, training junior staff and interacting with clients.

Manage all aspects of study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files, ensuring data quality, compliance with SOPs, regulatory requirements, and study completion on time and within budget.

Perform all aspects of CRA duties from site selection, site initiation, routine monitoring visits (on-site and remote), and close-out visits through to database lock. Be fully embedded in the client's study team and have a dedicated ICON functional manager to support you. Oversee all aspects of study site management to ensure high-quality data.