From study start up through implementation and reporting to close out, our Clinical Research Support Program (CRSP) unit offers flexible, cost-effective services to research teams across the lifecycle of a clinical study. Our goal is to provide a "Best Clinical Practice" environment, facilitating the highest quality clinical research and ensuring rigor and transparency. We offer expertise in NIH, industry, and investigator-initiated trials. 

CRSP Services

  • Start Up: Study design, feasibility, regulatory requirements, budgeting, contract negotiation
  • Implementation: Coordination; recruitment (from screening through consenting, enrollment, and scheduling visits to follow up); monitoring; data collection, entry, QC; specimen collection; helpful tools (sample logs, SOPs, checklists)
  • Reporting: ClinicalTrials.gov expertise, FDA and internal audit support
  • Publishing: Data sharing plan support to meet International Committee of Medical Journal Editor requirements
  • Close Out: Data archiving, financial close, contract close
  • Training: Our CRSP team comprises certified and highly experienced clinical research nurses, non-nurse coordinators, and regulatory and data personnel who provide guidance via educational workshops, drop-in clinics, and seminars. CRSP staff are also available as consultants or mentors on a per-hour, fee-for-service basis.

To find out about the latest learning opportunities as soon as they are announced, subscribe to CCTS Digest and check our Events and Recurring Events web pages.

Fees

Access a list of CRSP fees here (BlazerID & login required). 

Register

To register for a CRSP service, please fill in a CCTS Clinical Services form and submit it to This email address is being protected from spambots. You need JavaScript enabled to view it..

Don't see what you need? Have an urgent request? Contact us at This email address is being protected from spambots. You need JavaScript enabled to view it. or 205-934-7442.