Senior Clinical Research Associate (Chile)

Independently oversees all aspects of study site management to ensure patient safety is protected and quality of data is maintained. Conducts all forms of site visits, including pre-study, initiation, routine monitoring, and close-out visits. Prepares and submits accurate monitoring reports from all site visits and documents activities as per SOPs.

5+ years of experience in clinical research or related field. Strong knowledge of ICH-GCP guidelines and local regulations. Proven ability to manage complex clinical trials and mentor junior staff.