Clinical Research Coordinator - 236794

Job Summary: Coordinate and manage clinical trials to ensure compliance with protocols, regulations, and institutional policies, supporting participant safety and study integrity. Key Responsibilities: Facilitate site initiation and sponsor-required training for clinical protocols. Dispense study medications and coordinate with pharmacy staff as needed. Process and ship lab specimens in compliance with federal regulations. Conduct informed consent processes, ensuring proper documentation and compliance. Schedule and oversee study visits, tests, and procedures per protocol requirements. Accurately collect and report data, maintaining research subject charts and source documents. Perform or coordinate clinical procedures (e.g., blood draws, ECGs) with appropriate training. Report adverse events, protocol deviations, and violations to study sponsors and IRBs. Prepare and submit regulatory documents, including IRB applications and consent forms. Support participant recruitment, screening, enrollment, and retention. Serve as a liaison between participants, investigators, sponsors, and regulatory bodies. Assist in sponsor monitoring visits and audits, resolving findings promptly. Qualifications: 4 years as a Clinical Research Coordinator Oncology/ Cardiology experience preferred Phlebotomy Certification preferred Knowledge of clinical research protocols, GCP, and FDA regulations. Strong organizational, communication, and multitasking skills. Experience with clinical procedures and data management preferred. This role supports advancing research by ensuring high standards of protocol adherence and participant care.