Clinical Research Associate (Senior)

Role Overview: The Clinical Research Associate conducts site monitoring visits to ensure protocol compliance and high-quality execution of clinical trials. Key Responsibilities Perform site monitoring activities including selection, initiation, routine, and close-out visitsEstablish and maintain strong relationships with investigative sites to support study performance and recruitmentMonitor adherence to protocols, data integrity, and overall study qualityIdentify potential risks, resolve issues, and escalate concerns when necessaryTrack regulatory approvals, enrollment, and data quality metrics Qualifications & Skills Bachelor's degree in life sciences, healthcare, or related fieldMinimum of 1.5 years of on-site clinical trial monitoring experienceKnowledge of GCP, ICH guidelines, and regulatory standardsStrong communication, problem-solving, and organizational skillsAbility to manage multiple priorities in dynamic environments