Our Capacities

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1. Protocol Development / Medical Writing

From first draft of the protocol to CSR, we work congruently with your team to deliver.

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2. Site Selection/ Start up/ Regulatory

from best in class site selection to global regulatory needs on a local level

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3. Project Management

our project managers have worked on all sides of the industry to deliver key milestones

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4. Clinical Monitoring

Vetted and therapeutically aligned clinical research associates who are local language experts as well as primary site contacts throughout the lifecycle of trial

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5. Data Management

From database design and build to eCRF development and database lock, TRS has worked with multiple eCRF vendors to ensure a smooth deployment for both the sponsor and site

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6. Pharmacovigilance/ Safety

Safety database design , management and notification across the trial and globe per country regulations
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7. Medical Monitoring

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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