Tina N.

Experience

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  Indiana University

  Jan 1992 - Jan 2009

  Implemented and managed the new Indiana University Clinical Trials Office (CTO). Provided strategic leadership and oversight for expert research administration and regulatory compliance services for clinical research on all Indiana University campuses. Ensured that CTO services were delivered in a highly supportive model that promoted faculty research efforts while ensuring the Institution’s compliance obligations were met. CTO services included: proposal budget review; contract review, negotiation, and approval for all clinical research sponsored project agreements; and, post-award management. Personally responsible for negotiating the most complex and highest risk clinical research agreements with sponsors. Signed all clinical research sponsored project agreements on behalf of the Trustees of Indiana University. Show less

  • Director, Clinical Trials Office

    Jan 2003 - Jan 2009

  • Administrative Director, Wells Center for Pediatric Research

    Jan 1992 - Jan 2003
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  Dartmouth Hitchcock Medical Center

  Aug 2009 - Dec 2011

  Vice President for Clinical Research Operations

  Develop and lead the Clinical Research Division of Dartmouth-Hitchcock (D-H) including implementation of an institutional-level Clinical Trials Office (CTO), overseeing the processes, systems, educational programs, and other activities necessary to support growth and expansion of the clinical research enterprise at D-H. Oversee of the D-H Office of Intellectual Property Management and the Advanced Imaging Center. Provide financial oversight and management advice to the Graduate Medical Education (GME) and Center for Continuing Health Sciences Education (CME/CNE) offices. Serve as one of five members of the CTO’s Governance Board, a cross-institutional entity representing Dartmouth College, Dartmouth Medical School, SYNERGY (the Dartmouth CTSA), and D-H. Work collaboratively with the Dartmouth College Institutional Review Board and Office of Sponsored Projects to ensure clinical studies at D-H are performed in compliance with all applicable federal regulations. Represent and support D-H’s academic mission through engaged participation in senior leadership groups and committees. Show less

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  St. Vincent Hospital

  Dec 2011 - Aug 2015

  Director, Research and Regulatory Affairs

  Lead the Research and Regulatory Affairs departments of St. Vincent Health, overseeing all aspects of research compliance for this large, multi-site hospital system in Central Indiana. Direct the operations of the St. Vincent Institutional Review Boards (IRBs), and serve as the research administration and compliance expert for all sponsored research programs throughout the system. Member of the St. Vincent Corporate Responsibility Board, providing specific expertise on research compliance issues. Show less

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  St.Vincent Indiana

  Aug 2015 - Dec 2022

  Executive Director of Research

  Lead the strategic planning, resource allocation, and operational management of clinical research programs for St. Vincent Health, a large, multi-site Central Indiana health care system. Develop and lead business development activities for research services; build and maintain relationships with key stakeholders to advance the goals and objectives of the St. Vincent Health research program; promote research integrity and responsibility, including administrative oversight of the St. Vincent Health Institutional Review Boards. Serve on the St. Vincent Corporate Responsibility Board, providing specific expertise on research compliance issues. Show less

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  Ascension

  Dec 2022 - now

  National Senior Director for Human Research Protection

  Implement and lead the newly created Ascension Human Research Protection Program (HRPP) which consolidated all HRPP and IRB operations under a single national infrastructure.