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.