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Senior Clinical Research Associate
Clinilabs • US • published 2026-10-03 09:13:43.242311
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Description: **JOB SUMMARY** The Senior Clinical Research Associate (SCRA) is responsible for monitoring clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, sponsor requirements, and applicable regulatory standards. The SCRA serves as a primary liaison between investigative sites and the study team, supports study start\-up and site management activities, conducts monitoring visits, utilizes electronic systems, reviews study documentation, and contributes to the successful execution of clinical trials. **RESPONSIBILITIES** * Review study protocols, Investigator Brochures, Clinical Monitoring Plans, and study\-related documents to ensure a thorough understanding of study requirements and objectives. * Conduct site qualification, initiation, routine monitoring, and close\-out visits in accordance with study protocols and approved Clinical Monitoring Plans. * Assess investigator qualifications, site capabilities, patient populations, and facility resources to determine site suitability for study participation. * Serve as the primary contact and resource for assigned investigative sites....
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