Clinical Trial Support


Our SRC clinical trial experts and outstanding project management skills help us meet your goals and timelines.   We will work with you to find the right combination of professional services based on your needs and our extensive experience.  Our success is based upon working closely with your existing team and developing a customized approach to efficiently meet your specific clinical trial needs.

Our clinical trial support services include:

  • “Hands-on” oversight from concept to completion
  • Prepare clinical project deliverables: Protocol, Informed Consent & CRFs
  • Identification and GCP qualification of clinical sites
  • Investigator Meeting planning and conduct
  • Prepare regulatory documents and interface with IRB
  • Site personnel training and clinical trial monitoring
  • Safety review by our medical staff
  • Pharmacovigilence and Adverse Events management
  • Comprehensive clinical study report writing (See Medical Writing Services)

Contact our experts.