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Our Services

Our Services

Clinical Trials Division coordinates and facilitates access to promising new therapies, quality research standards, and efficiencies in the conduct of clinical trials.

  • Sponsor and Contract Research Organization (CRO) contacts.
  • Institutional Review Board application support.
  • Budget Development and contract negotiations.
  • Site initiation and management.
  • Regulatory support.
  • Quality and compliance review.
  • Clinical Trials staff research training and tracking.
  • Personnel recruitment support.

What do our Clinician Investigators do?

  • Act as Principal Investigators for clinical trials research.
  • Develop ideas and protocols for new clinical research projects.
  • Make scientific presentations at professional meetings.
  • Author manuscripts for peer-reviewed journals.
  • Provide expert support for clinical program development plans and FDA and international
    regulatory meetings.

Site Management

Clinical Trials Division offers site management support, including

  • Investigator qualification/selection and site recruitment.
  • Investigative site start-up and training.
  • Facilitation of clinical trial enrollment.
  • Ensuring site regulatory compliance.
  • CRF completion, data collection and query resolution.
  • Expedited adverse-event reporting.