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Office of Clinical Research

Information for Investigators and Departments [Intranet; internal access only]

Information for Industry Collaborators

Contact Us:


Meg Johnson, JD, CIP
Director, Office of Clinical Research

Clinical Research Agreements and Budgets   

Debra Strandberg
Contract Administrator III, Sr. Contract Administrator

Overall agreement management, support and assistance, master agreements


Elena Del Prete, MS, MBA
Contract Administrator II, Budget Specialist

Clinical research agreements, budgets and financial review and assistance, cross-support to terms specialist as needed


Cara Martinoli, JD
Contract Administrator II, Terms Specialist

Clinical research agreements, CDA review, DUA/DTA review, terms and conditions review, cross-support to budget specialist as needed

Human Research Protection Program (HRPP) Quality Improvement/Quality Assurance and Education Program

Terry Sousa, RN, MSN, CCRC, CIP
Quality Improvement Manager

Post-approval monitoring for the Human Research Protection Program, directed/for cause audits, HRPP QA/QI, full monitoring services as requested


HRPP Educator/Education Specialist III

Support and facilitation of HRPP educational initiatives including: Good Clinical Practice, Clinical Research Professionals Group, general education on HRPP and clinical research best practices