Clinical Research Training Course for Clinical Faculty

An important focus for the University at Buffalo and the UB Clinical and Translational Science Institute (CTSI) is expansion of the clinical and translational research workforce including investigators, coordinators, and staff, by providing user-friendly training opportunities and mentoring. Faculty revealed in a survey their interest in conducting clinical research and identified lack of training and mentoring as key obstacles. Another survey of Buffalo Translational Consortium faculty and research coordinators identified a need for practical training. 

Formal course work and instruction delivered in person requiring several continuous hours of commitment is not feasible for most clinical faculty and staff. The Clinical Research Training Course for Clinical Faculty is an asynchronous training model that can be integrated in workflows with minimal disruption. 

Prerequisites:  

Institutional Review Board (IRB) required Collaborative Institutional Training Initiative (CITI) Researcher Training (available at ):

  • Biomedical Research Investigators Course OR Social & Behavioral Research Investigators Course 
  • Good Clinical Practice Course
  • Conflicts of Interest

Optional but recommended CITI courses:

  • Health Information Privacy and Security (HIPS/HIPAA)
  • Clinical Trial Billing Compliance (CTBC)

Instructions for CITI access and the listing of required course work may be found here: 

Course components:

Educational Videos Meet and Learn Shadowing Mentored Experience

Meet and learn with research support staff within the Clinical Research Office (CRO) and additional research offices as needed

The clinical faculty member will be invited to meet with the following CRO/CTSI personnel on a one-to-one basis to develop a good grasp of establishing and running a clinical research project, and identify individuals to work with subsequently.

Person Area of expertise
Marchelle Brooks, MPH, or Alexis O’Brien
Clinical Research Facilitators
Link researchers with research support 
Sanjay Sethi, MD, FACP
CRO Medical Director
Overview of support resources
Pamela Anderson, RN, BSN 
Associate Operational Director
Post award (finances, HR)
Kimberly Brunton, RN, MSN
Associate Operational Director
Pre award (clinical study registration)
Lynn Jagodzinski
Clinical Research Regulatory Administrator
Regulatory (IRB submission, IND, IDE)
Rosanne Johnson
Clinical Research Budget & Coverage Analyst
Budget (creation, negotiation)
Mariya Cherneva, MA
Clinical Trials Management System Specialist;
UB Senior OnCore Coordinator
Oncore (clinical trial management system)
Ashley Regling, MA
Clinical Recruitment Coordinator
Recruitment (methods, toolkit)

Based on the nature and location of their subsequent work as a clinical investigator, arrangements will be made for meetings with additional research offices such as the IRB, Sponsored Projects Services (SPS), Office of Clinical Trial Development and Implementation (OCTD), as well as with other personnel within the CRO or the CTSI.  

Contact the Program Coordinators to register for this course:

Alexis O’Brien 
ahazard@buffalo.edu 
716-829-4357

Marchelle Brooks, MPH 
mbrooks9@buffalo.edu 
716-829-4357

To begin the Clinical Research Training Program, reach out to a Program Coordinator. Once training is complete, a Completion Certificate will be awarded to the trainee.