Clinical Research Coordinator II

Classification Title:

Clinical Research Coord II

Job Description:

The ImagingNMD UF research team brings researchers from across the University of Florida campus, industry, and other institutions in a collaborative effort to advance the understanding and treatment of neuromuscular diseases, including Duchenne, Beckers, and Limb Girdle Muscular Dystrophies. This team facilitates clinical research studies and trials focused on neuromuscular diseases and is engaged in national and international collaborative research efforts. The ImagingNMD network is seeking a diligent, detail-oriented, and experienced individual to serve as the Clinical Research Coordinator II for these critical clinical research studies.

This full-time position within the Department of Physical Therapy, in the College of Public Health and Health Professions, is located in the Clinical Translational Research Building, at the University of Florida. The incumbent will work closely with principal investigators (PIs) and faculty to facilitate the implementation of research activities for both industry and NIH-sponsored clinical studies, focusing on interventional and non-interventional trials related to muscular dystrophy.

The incumbent will collaborate with principal investigators to efficiently coordinate participant assessments, and maintain data collection records for multiple federally and industry-sponsored clinical trials.. As a member of the ImagingNMD network, the Clinical Research Coordinator II works closely with investigators, physicians, nurses, and other key personnel to ensure compliance with protocol requirements. Primary responsibilities involve coordinating the clinical research activities of the ImagingNMD network, including assisting in the development of procedural manuals, scheduling research participants, facilitating key elements of study protocols, training research assistants, and maintaining compliance with regulatory bodies. Furthermore, the incumbent will serve as the primary liaison with national and international imaging sites within the ImagingNMD network and be responsible for maintaining vendor regulatory and participant visit related documents.