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Catherine Hackett Renner, PhD
Director
Responsible for the operation of the Office of Research and oversees feasibility and progress of all clinical trials.
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Brian Sheesley, MPA
Director of Sponsored Programs
Assists with grant application development and post-award administration.
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Deanna Nobis, CRCP
Contracts and Regulatory Coordinator
Responsible for preparing, reviewing and negotiating legal documents for clinical trials.
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Tracy Bemis
Contract and Regulatory Coordinator
Responsible for negotiating the budget and overseeing the financial aspects of clinical trials and the Office of Research.
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Danielle Hahn, BS
Clinical Research Coordinator
The Certified Clinical Research Coordinator will assist Principle Investigators in the conduct of the study, schedule subject visits, complete visit activities, complete source documents and case report forms, meet with study monitors and attend procedures.
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 | | Hannah Eubanks, MHA Clinical Research Associate Responsible for regulatory and IRB submissions for the Clinical Trials Office.
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 | | Heather Nolting, BSN, RN
Clinical Research Coordinator The Certified Clinical Research Coordinator will assist Principle Investigators in the conduct of the study, schedule subject visits, complete visit activities, complete source documents and case report forms, meet with study monitors and attend procedures.
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 | | Heather Banker, MS
Clinical Research Coordinator The Certified Clinical Research Coordinator will assist Principle Investigators in the conduct of the study, schedule subject visits, complete visit activities, complete source documents and case report forms, meet with study monitors and attend procedures.
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Michelle Pennington
Secretary
Secretarial duties and assist with special projects for the office.
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