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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 @ Maureen.Hurst@stonybrookmedicine.edu  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

Note-to-File

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