Director-Research Administration, The Neuroscience Research Institute, The Ohio State University

Director-Research Administration, The Neuroscience Research Institute, The Ohio State University

Personal Statement: Beginning in 1988 I have been involved in the development, coordination, management and administration of various publicly or privately sponsored, single or multicenter, clinical or epidemiological research projects. From 2002-2015, I served as the research subject advocate (RSA) for the Clinical Research Center at The Ohio State University. Over that time, I also served on numerous Data & Safety Monitoring Boards (DSMB). From 2008 through 2015, I served as an in-house Clinical Research Consultant for the Center for Clinical and Translational Science, a NIH-CTSA site, providing regulatory and research ethics protocol development, IRB submission and study monitoring support and was actively engaged in various related CTSA Consortium and university initiatives, including the Ohio Reliant IRB Consortium and the National CTSA Reliant IRB Collaboration. Currently, I serve as the administrative director for the NRI at Ohio State, facilitating research best practices and collaborations for 180+ faculty and 40 clinical research staff. Through my various university activities, I have established viable relationships with the Ohio State Offices of Research, FCOB Center for Operational Excellence, Research Compliance, Sponsored Programs and Responsible Research Practices, and various OSUWMC task forces. I also serve as an institutional expert on DSMBs, and serve co-chairman of a CTSA DSMB workgroup.

Positions and Employment:

1988-1990 Program Coordinator, Epilepsy Program, Department of Neurology, The Ohio State University
1991-1993 Program Manager, Epilepsy Program, Department of Neurology, The Ohio State University
1993-1998 Project Director, Epilepsy Program, Department of Neurology, The Ohio State University
1999-2001 Research Specialist, Parkinson Program, Department of Neurology, The Ohio State University
2002-2005 Adjunct Faculty, Department of Human Services Management, Franklin University
2002-2015 Research Subject Advocate (RSA), Clinical Research Center, The Ohio State University
2005-present Adjunct Assistant Professor, College of Public Health, The Ohio State University
2005-2008 Instructor, COM NIH T32 Award: Training in Clinical Investigations
2008-2015 Clinical Research Consultant/RSA, Center for Clinical and Translational Science, The Ohio State University
2010-present Adjunct Research Professor, OSU College of Nursing
2015-present Administrative Director, Neuroscience Research Institute

Other Experiences and Memberships:

1997-2001 American Society for Experimental Neurotherapeutics (founding member)
2002-2009 Member/Secretary, Society of Research Subject Advocates
2004-2010 OSU College of Medicine Professionalism Council’s Committee on Research Ethics
2004-2010 OSU Hospitals Subcommittee on HIPAA and Research Conduct
2006-present DSMB member/Independent Safety Officer: various not-for-profit and NIH-funded studies
2008-2012 OSUWMC Ross Heart Hospital Biobank Steering and Scientific Review Committee
2008-2014 CTSA Regulatory Knowledge Committee (non-voting)/Research Subject Advocate Task Force
2008-present CTSA Research Ethics Committee (voting)/Operations Committee/Consultation Task Force
2011-present CTSA RKS KFC Monitoring/DSMB Affinity Group, Co-Chairman
2011-present Health Improvement Institute: Award Judge
2012-present OSU CON Grant Mentoring Committee
2013-present Reviewer, Annals of Epidemiology
2013-2015 Midwest Area Research Consortium for Health, Operations, and DSMB Task Forces
2014-present OSU Medical Center Research Data Management Task Force
1982 Chi Gamma Nu, Chemistry Honors, Ohio Wesleyan University
2012 Health Improvement Institute: CCTS Human Research Protection Program, Certificate of Merit
2013 OSU Staff Development Award recipient
2015 OSUWMC BRAVO Values in Action Award recipient


Reider CR, Hubble JP, Harrold B. Risk factors in PD: a matched pair study. Parkinsonism and Related Disorders 1999;5(Suppl 1): S47.

Reider CR, Rice R, Grever J. A web-based protocol development timeline- the OSU experience. CTSA Consortium CRM/RKS Annual Meeting 2009.

CTSA IND/IDE Taskforce. IND/IDE Taskforce: a year in review. CTSA Consortium CRM/RKS Annual Meeting 2010.

CTSA Study RegistrationTaskforce. Requirements: a survey of CTSA Institutions’ Administrative Practices. CTSA Consortium CRM/RKS Annual Meeting 2010.

OSU CCTS Clinical Research Support Team. Three Complementary Research Subject Recruitment Strategies. CTSA Consortium CRM/RKS Annual Meeting 2010.

Reider C, Carpenter D, Borlowsky T. StudySearch: An Open source searchable tool for listing studies recruiting human subjects. CTSA Consortium CRM/RKS Annual Meeting, 2012.

PHS 398/2590 (Rev. 09/04) Page Continuation Format Page
Hallarn RK, Para M, Reider C. OSUMyChart: Using a Patient Platform to Promote Participation in Research. CTSA Consortium CRM/RKS Annual Meeting 2013.

Reider C, Cola P, Strasser J. The Ohio CTSA Consortium Reliant IRB Agreement. CTSA Consortium
CRM/RKS Annual Meeting 2013.


Reider CR. Orphan Drug Act: Provisions and considerations. Drug Information Journal, 2000;34:295-300.

Reider CR, Hubble JP. Test-retest reliability of an epidemiological instrument for Parkinson’s disease. Journal of Clinical Epidemiology, 2000;53:863-865.

Reider C, Halter C, Castellucio P, Oakes D, Foroud T, and the Parkinson Study Group. Reliability of reporting age at onset for Parkinson’s Disease. Movement Disorders, 2003;18(3):275-279.

Reider C, Malarkey W, Nagaraja, H. GCRC Subject Satisfaction Survey. Journal of Clinical Research Best Practices 2007;3(1):1-6.

Beskow LM & the CTSA Clinical Research Ethics Consultation Taskforce. Points to Consider: The Research Ethics Consultation Service and the IRB. IRB: Ethics & Human Research 2009:31(6): 1-9.

Johnson T, Joyner M et al. Using research metrics to improve timelines: proceedings from the 2nd Annual CTSA Clinical Research Management Workshop. Clin Transl Sci 2010:3(6):305-308.

Berro M, Burnett B & the CTSA IND/IDE Taskforce. IND/IDE Support for Investigator-Initiated Clinical Research: The Clinical and Translational Science (CTSA) Experience. Academic Medicine 2011:86(2):217-223.

Carpenter D, Kelsey B, Rice R, Reider CR, Borlawsky TB. StudySearch: A Tool For Connecting Potential Participants with Locally Recruiting Studies. AMIA Summits Transl Sci Proc. 2011 Mar.

Kang UJ, Auinger P and the PSG ELLDOPA Investigators. Activity enhances dopaminergic long-duration response in Parkinson disease. Neurology 2012:78(15):1146-1149.

Kost R, Reider C, Stephens J and the CTSA RSA Taskforce. Research Subject Advocacy: Practice and Impact at NIH Clinical & Translational Science Award Sites. Academic Medicine 2012:87(9): 1228-1236.

McCormick J, Sharp R, Ottenberg A, Reider C, Taylor H, Wilfond B. The Establishment of Research Ethics Consultation Services (RECS): An Emerging Research Resource. Clinical and Translational Science 2013:6(1): 40-45.

Cola P, Reider C, Strasser J. The Ohio CTSA Consortium Reliant IRB Model for multi-center clinical research. Clinical and Translational Science 2013: June 2013.
Cho M,; Taylor H, McCormick J, Barnard D, Boyle M, Capron A, Dorfman L, Havard M, Reider C, Robinson M, Sandler J, Schwartz P, Anderson N, Danis M, Sharp R, Wilfond B. Building a Central Repository for Research Ethics Consultation Data: A Proposal for a Standard Data Collection Tool. Clinical and Translational Science (accepted 1/2015)

Gonsenhauser B, Hallarn B, Carpenter D, Para M, Reider C. StudySearchTM: a web-based application for posting and searching clinical research studies. Journal of Investigative Medicine (submitted 11/2015).

Reider, C. “Educating to Protect.” Applied Clinical Trials, February 2005: 14.

Completed Support:
CTSA-UL1TR001070- Rebecca Jackson (PI) 100% 05/01/2013- 08/31/2015
NIH/NCRR - Clinical and Translational Science Award

CTSA- UL1RR025755-Rebecca Jackson (PI) 100% 05/19/2008- 04/30/2013
NIH/NCRR - Clinical and Translational Science Award

M01-RR00034-37 – Wiley Souba (PI) 100% 12/01/2006- 11/30/2009
NIH/NCRR - General Clinical Research Center

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