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Office of Clinical Research

About Us

Navigating the study start-up process for clinical research can be challenging. The Office of Clinical Research (OCR) at MUSC partners with study teams and research-related offices across the MUSC enterprise to ensure research billing compliance and improve the financial and operational performance of clinical research.

Our Mission

The OCR serves as a hub for the MUSC research community, offering resources, systems, services, and training from our core teams.

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What We Do

  • New Study Opportunities: We disseminate new study opportunities to keep our research community informed.
  • Study Feasibility Support: We offer feasibility support and pre-site visit assistance to ensure successful study initiation.
  • Compliance Guidance: Our team guides investigators to meet federal research billing compliance regulations with comprehensive protocol reviews and Coverage Analysis (CA) development.
  • Budgeting and Negotiations: We reduce study staff burden by leveraging our experienced corporate clinical research budgeting and negotiations fee-for-service team.
  • Revenue Collection: We maximize revenue collection with centralized fee-for-service invoicing expertise for corporate clinical research.
  • Financial Management: We streamline financial management and study tracking with the institutionally mandated OnCore Clinical Trial Management System (CTMS).
  • Patient Payments: We offer a secure way to disburse payments to research patients in real-time with ClinCard reloadable debit cards.
  • ClinicalTrials.gov Compliance: We collaborate with study teams to ensure compliance with federal registration, record maintenance, and results-reporting requirements.
  • Research Professional Networking Group: We created the Research Community Hub (RCH) to provide a supportive space for MUSC research staff to share information, ask questions, and foster connections with other research professionals to enhance research excellence across our institution.

Collaboration Information for Clinical Research Sponsors & Contract Research Organizations (CROs)

Industry Sponsors & CROs

The OCR is very knowledgeable about billing/coding which has been very helpful in negotiating budgets with sponsors.

Debi Everidge Cardiology

Meet Our OCR Leadership

Royce Sampson, MSN, RN, CRA
Director, OCR;
Administrator, SCTR;
Project Director, Research Expansion
sampsonr@musc.edu

Signe Denmark, MS, CCRP
Associate Director, Research Opportunities and Collaborations (ROC) and Finance
denmarks@musc.edu

Leila Forney, DNP, CCRP, CHRC
Associate Director, Prospective Reimbursement Analysis (PRA)
forney@musc.edu

Stephanie Gentilin, MA, CCRA
Associate Director, Human Subject Regulations
mamaysl@musc.edu

Kelly Hickman
Associate Director, Communication and Development
hickmank@musc.edu

Steven Shapiro, MHA, MSHI, PMP
Associate Director, Clinical Trial Management Systems (CTMS)
shapirsb@musc.edu

MUSC Health/RHN Research

Investigators can expand their research reach with the support of the MUSC Health/Regional Health Network (RHN) centers located in Columbia, Florence, Lancaster, and the regional medical center in Orangeburg. Visit the MUSC Health/RHN website to learn more about these centers' patient populations, specialty areas, resources, and services.

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