Research Management

Regional Health Clinical Research provides all inclusive research services to Principal Investigators conducting research from study start to study completion, including:

- study cost analysis
- budget formulation
- billing
- lab
- pharmacy
- clinic/floor
- reporting requirements
- submission forms
- informed consent
- Human subject protections
- Good clinical practice
  • Identifying research opportunities
  • Research coordination such as implementation and administration of clinical studies
  • Regulatory oversight
  • Provision of financial services for new studies:
  • Coordination of contract negotiations
  • Oversight of research participant registration and research billing
  • Assistance and coordination with study advertisement and patient recruitment
  • Part 11 compliant
  • Secure, temperature-monitored investigational product storage
  • Developing study procedures:
  • Oversight of the submission process to the Institutional Review Board (IRB), to include Central or Local IRB:
  • Quality research initiative including:
  • Compensation for serving as an investigator

Investigator participation

While there are responsibilities that come with serving as a Principal Investigator, there are many rewarding reasons for participating in clinical trials, including:

  • Providing cutting-edge therapies to your patients
  • Contributing to the advancement of health care
  • Staying in touch with the latest in medical science
  • Identifying research studies
  • Compensation for fulfilling research responsibilities
  • Educational opportunities

Call (605) 716-3982 if you are interested in any of our clinical trials.

Click for Current Clinical Trials