Clinical Research

Concierge Home | Bioinformatics | Biostatistics | Clinical Research | Metabolomics

The Clinical Research Concierge provides assistance to (a) investigators with little or no clinical research experience and (b) for projects that may or may not have funding or a protocol in place for newly approved or in-progress clinical and translational research studies.


Services

  • Developing new study designs and reviewing proposed study designs
  • Identifying qualified clinical collaborators and research resources
  • Preparation of IRB and other regulatory documents (safety monitoring plans and interim reports)
  • Navigation through the IRB approval process
  • Training on accessing and using the UNC Clinical and Translational Research Center
  • Development of study-related materials (consent forms, recruitment materials, case report forms)
  • Assistance with writing the human subjects section of grant applications
  • Problem solving for issues such as subject recruitment strategies, compliance, and data safety monitoring

Contact

fischer_leslie

Leslie Fischer, PhD, Clinical Research Concierge

Research Assistant Professor
Department of  Nutrition 
T: (919) 408-3320
E: lfischer@email.unc.edu


Service Request Form
To request clinical research concierge services, please complete the online service request form.