Senior Clinical Research Associate - Early Clinical Development

Role Overview: A Senior Clinical Research Associate is responsible for managing early-stage clinical trials, primarily in Phase 1, on the East Coast. Key Responsibilities Conduct site visits including site selection, initiation, monitoring, and closeout activitiesCollaborate with site staff to develop recruitment strategies and monitor enrollmentProvide protocol training and maintain ongoing communication with site personnelEnsure protocol adherence, data quality, and regulatory complianceMaintain essential documents in Trial Master Files and Investigator Site Files according to standards Qualifications & Skills Bachelor's degree in life sciences or health-related fieldAt least 1.5 years of on-site clinical trial monitoring experienceStrong knowledge of GCP, ICH guidelines, and regulatory requirementsWillingness to travel as needed