Clinical Research Coordinator

We are looking to add a full time onsite Clinical Research Coordinator to a growing research site. Qualified candidates will have a minimum of 1 year of experience working on Sponsor funded studies and must be able to perform phlebotomy. Responsibilities Performs study subject visits, Screening and recruiting subjects; Dosing and administering study drugs and/or implementing study methodologies Collecting, labeling, storing, and shipping specimens collected from subjects in connection with a clinical research trial Entering patient and research data in systems designated by the Company Maintaining patient charts and resolving research queries. Monitors study activities to ensure compliance with study protocols and with applicable federal, state, and local regulatory and Site requirements and policies; Maintains required records of study activity including case report forms, drug dispensation records, and regulatory forms; Oversees subject enrollment to ensure that informed consent is properly obtained and documented Records adverse events and side effect data and confers with Investigators regarding the reporting of events to oversight agencies Documents findings and events in the Company’s research CTMS platform and in other binders and platforms as directed #J-18808-Ljbffr