Clinical Research Coordinator
Current• Enrolling and recruiting patients for clinical trials, covering informed consent, conducting eligibility screening, data collection and ensuring inclusion of the subjects are adhering to safety and study protocols.•Provide potential patients/participants with study information.•Conducting research visits and collecting/shipping biological specimens for analysis according to protocol requirements and submitting necessary paperwork to the sponsor.•Maintaining source documents and subject files in accordance with practice procedures and ensures accurate and complete compilation of subject data through chart reviews.•Adhering to Good Clinical Practice and complying with Institutional, State, and Federal regulations throughout the study.