Our Capacities

We are proud to provide the following services:

1. Protocol Development / Medical Writing
From draft idea to full protocol and CSR
2. Site Selection/ Start up/ Regulatory
From initial site identification to country specific regulatory needs, TRS has successfully launched trials in 43 countries
3. Project
Process driven project management to deliver key study milestones on time, every time
4. Clinical
Vetted and therapeutically aligned clinical research associates who can are local language experts as well as primary site contracts throughtout lifecycle of trial
5. Data
From database design and build to eCRF deployment and database lock, TRS has worked with multiple eCRF vendors to ensure a smooth deployment for both the sponsor and site
6. Pharmacovigilance/ Safety
Safety database design , management and notification across the trial and globe per country regulations
7. Medical
24 hour therapeutically aligned physician management and leadership to ensure translational protocol adherement.
Submit a RFP

A large part of NC's CSO industry is made up of contract research organizations (CRO) and companies that are focused on clinical trial management. The North Carolina CRO Collaborative was brought together to address and support the needs of the companies who operate in this subsector.

The immediate goals of the CRO Collaborative are to improve and expand clinical-based workforce development in North Carolina through curriculum enhancement and development as well as increase awareness of CRO industry trends and career opportunities throughout the state.

The committee is comprised of representatives from eight CROs, eight academic institutes (both clinical research training programs and university-affiliated clinical site programs), supporting institutions, and one hospital system. 

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