research Services

You know medicine.  

We know the business of clinical research.  

Principle Research Solutions will provide all necessary elements required  to run successful clinical research trials including;  the necessary staff to effectively execute the protocol, regulatory document submission and compliance, contract and budget negotiation, maintenance of accurate financial records for each study, and post study document storage/archival.

Complete trial execution from your office/clinic.  Our staff will work at your site and all visits will occur in your facility eliminating the need for you to be away from the office and unavailable to your own clinic patients. Our staff works with your staff for scheduling and patient flow.

Our Clinical Research Coordinators are all trained and certified with International Conference of Harmonization and Good Clinical Practices.   

(ICH / GCP E6 R2) 

Coordinators also maintain current IATA Dangerous Goods Regulations certificates.  

Business development from the ground up.  Trial opportunity and procurement.

PRS obtains, completes and submits feasibility forms from all sources.

Attend meetings and acquire all materials needed for a successful start of trial.

Meet and review with CRA/Project Manager from Sponsor/CRO.

HR is a breeze with PRS.  Allow our team to headhunt, interview, screen and hire staff for you.   

Up-to-date education and training are a necessity. Let PRS train your staff.  Keep current on GCP, IATA, and grow your current staff's expertise with the industry's best Clinical Research Coordinator (CRC) training.  

Our decades of experience bring you written SOP's and guidelines that are easy to follow and address real world scenarios.

Provide support and representation in the event of an audit by sponsor or regulatory authorities.

We would appreciate the opportunity to present customized SOLUTIONS for your research practice. For more information or to schedule a meeting please contact Christi Witte, CMA, CCRC at (509) 496-2782 (voice/text)