Job Summary:  Coordinates the management of clinical trials including identification of participants, coordinating their study related care throughout the trial, and following the trial participants long term as study protocol dictates. Maintain confidentiality, HIPAA compliance and ensure protection of participants enrolled in clinical trials.  Ensure that scientific integrity is maintained through data reliability and strict adherence to regulatory mandates.  Adherence to CaroMont Health established IRB policy and protocols.  Other duties in support of the Office of Research Administration as assigned. 

Qualifications:   Bachelor’s degree in a science-related discipline required. Clinical research required. BLS required within three (3) months of employment. Research Regulatory experience strongly preferred. Research certification required within (3) years of employment (e.g. SoCRA or ACRP).  Must be proficient with Microsoft Word and Excel.  Ability to work autonomously and in teams as required.  Demonstrates good multitasking, organizational, and communication skills.  Periodic travel required (<5%).

EOE AA M/F/Vet/Disability