Clinical Research Coordinator

Coordinates, supports and facilitates the daily clinical trials activity and plays a c

Core Duties and Responsibilities:

• Coordinates, supports and facilitates on site, as well as at home (remote) clinical studies in strict accordance with approved protocols
• Conducts research in accordance with Good Clinical Practice (GCP), Life Extension Clinical Research Standard Operating Procedures, Policies and Work Instructions as well as applicable local, state, and federal regulations

• Performs clinical tasks including, but not limited to, managing study products, laboratory specimen storage/shipment, adverse event documentation and reporting in a timely manner
• Responsible for data management and integrity ensuring that the transfer of the data from the source documents and laboratory reports to a data template and case report form, if needed, is completed in a timely manner
• Assists with the collection of data, correspondence and submissions to the Institution Review Board (IRB) and other regulatory agencies, as needed

• Facilitates study close out activities and retains records/archives documents, as required
• Identifies, reports, and provides solutions for preventing any protocol deviations while escalating any quality or subject safety concerns per departmental policy and in adherence to IRB requirements
• Flexibility to travel outside of the facility to recruit potential subjects (i.e., physician offices, health fairs, expos etc.), deliver study products to outside sites as well as provide monitoring type services for the Life Extension sponsored clinical studies, as needed
• 2 onsite days per week is an essential function of this position after completion of the introductory period
• Other duties and responsibilities as assigned

Position Requirements: