Senior Clinical Research Associate

Responsibilities: of the Senior Clinical Research Associate (SCRA): • Serve as the primary point of contact between investigational sites, sponsors, and internal study teams. • Conduct Site Selection, Initiation, Monitoring, and Close-Out Visits in accordance with study requirements and ICH GCP guidelines. • Build and maintain strong relationships with investigators and site personnel to support study execution, enrollment goals, and protocol compliance. • Verify subject safety, informed consent, investigational product accountability, and data accuracy through source document review and site monitoring activities. • Ensure study documentation, Trial Master Files, and clinical trial management systems remain accurate, complete, and inspection-ready. • Provide routine study updates, monitoring reports, and issue escalation to project leadership as needed. Requirements of the Senior Clinical Research Associate (SCRA): • 3-5+ years of Clinical Research Associate experience within the clinical research industry. • Bachelor's degree in Life Sciences, Healthcare, Clinical Research, or a related field preferred. • Strong knowledge of ICH GCP guidelines, clinical trial regulations, and monitoring best practices. • Experience conducting onsite and remote monitoring visits across multiple phases of clinical trials. • Excellent communication, organizational, and relationship-management skills. Compensation: for the Senior Clinical Research Associate (SCRA): • Pay Rate: $80.00/hour • Comprehensive Benefits: Medical, Dental, Vision, 401(k), Paid Time Off, Sick Leave (as required by law), and Paid Holidays