Sr. Clinical Trial Associate

We are seeking a Sr. Clinical Trial Associate with experience supporting clinical trials, study coordination, and clinical operations. Responsibilities: Maintain Trial Master Files (TMF) Support IRB submissions and study documentation Coordinate clinical trial activities and site communications Perform CTMS data entry and tracking Support investigator meetings and study start-up activities Track monitoring reports and clinical supplies Requirements: Clinical research / clinical trial experience Experience with TMF, CTMS, IRB submissions, and study tracking Knowledge of GCP / ICH guidelines Strong organizational and communication skills CRO, biotech, pharma, or healthcare research background preferred Ideal backgrounds: Clinical Trial Associate (CTA) Clinical Research Coordinator Clinical Operations Coordinator TMF / Regulatory Coordinator Apply today or reach out for more information.