Updated:TodayLocation:Tlalnepantla, MEX, MexicoJob ID:********This Clinical Research Associate (CRA I) role involves overseeing the integrity of clinical research studies by conducting site qualifications, monitoring, and ensuring compliance with regulatory and protocol standards.Job ResponsibilitiesPerform site qualification, initiation, interim monitoring, site management activities and close‐out visits (on‐site or remotely) ensuring regulatory, ICH‐GCP, Good Pharmacoepidemiological Practices (GPP) and protocol compliance; evaluate overall site performance, recommend actions and develop action plans.Verify informed consent procedures are adequately performed and documented; protect confidentiality; assess factors that might affect subject safety and data integrity.For the Clinical Monitoring/Site Management Plan (CMP/SMP):Assess site processes.Conduct source document review of site records and medical documents.Verify required clinical data entered in the case report forms (CRFs) ...