Do you need help implementing your trial protocol but can't afford another full-time employee? Our CRSP team comprises trained, certified, and experienced research nurses, non-nurse coordinators, and regulatory and data personnel who can help fill in the gaps on your research team. You pay only for the amount of effort required. 

Outsource for Success

We provide the following implementation services in clinical trial and human subject studies:

• identifying, pre-screening, and enrolling eligible participants
• recruitment and informed consent
• monitoring participants/records
• study visits
• collecting specimens
• collecting and entering data (see our Research Commons domain for data management support)
• maintaining regulatory and financial records
• submitting protocol amendments

CRSP also offers a Clinical Trials Kiosk of helpful implementation tools, including logs, checklists, and standard operating procedures. 

Register

To register for a CRSP service, please fill in a CCTS Clinical Services form and submit it to This email address is being protected from spambots. You need JavaScript enabled to view it..

CCTS Research Commons offers additional support for study implementation, including access to clinical data, bioethics consultations, and unique CCTS Partner Network resources. Don't see what you need? Have an urgent request? Contact us at This email address is being protected from spambots. You need JavaScript enabled to view it. or 205-934-7442.