Trials Innovation Consultation

The CTS team provides resources to accelerate and streamline clinical research trial start-up, recruitment, retention, study management and integration of research in the clinical setting.

Available services include:

  • Provide educational programs, training and consults to strengthen career development among principle investigators and research staff in clinical and translational research. 
  • Serve as a knowledgeable resource to clinical researchers and serve as a liaison to the existing clinical trial resources and research offices regarding trial start-up, recruitment, retention, and study management.
  • Work with research offices at Stony Brook such as the Office of Research Compliance, Office of Scientific Affairs and Office of Sponsored Programs. 
  • Assistance with funding opportunities, clinical trials budgeting, proposal submissions, IRB submissions and project management. 
  • Systematically collect and report metrics related to study start up and enrollment of clinical research trials for the purposes of review and process improvement.
  • Support Stony Brook investigators to conduct multi-center trials and IRB process through SmartIRB.

Consult with an expert!

The support services are provided by Lead Knowledge and Clinical Trials Specialist, Maureen Hurst so call now!!!

To request a consultation please use the Stony Brook CTS Consultation Request Form.docx

For clinical trial questions, contact Maureen Hurst LPN, BS, MHA, CCRC @  or call 631-638-1942

Useful CTSC Templates 

Stony Brook CTSI Consultation Request Form.docx

Adverse Event Log

Concomitant Medications

Delegation of Responsibility Log

Data Safety Monitor Board Log

Inclusion/Exclusion Checklist

Informed Consent Process

Informed Content Tracking Log

Informed Content Change Tracking Log

Investigational Product Accountability Log-Stock Record

Investigational Product Accountability Log-Subject Record

Master Subject ID Log

Monitoring Visit Log


Participant Enrollment

Protocol Deviation Tracking Log

Protocol Amendment Tracking Log

Serious Adverse Event Log

Screening and Enrollment Log

Specimen Tracking Log

Study Notes

Training Log