SC Liver Research Consortium

Your Link to a Successful Clinical Trial
Company
SC Liver Research Consortium is an organization of physicians specializing in hepatology and gastroenterology clinical research. Our mission is to team research sponsors and our network sites together to provide faster, higher-quality research results.
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Services
SC Liver Research Consortium provides input on clinical trial design, project management, site selection, and subject recruitment. Our team serves on Advisory Boards and Data Monitoring Committees. We sponsor several national CME training programs.
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Experience
SC Liver Research Consortium partners with large and small pharmaceutical companies and CROs, to design effective clinical trials, select appropriate sites, expedite start-up, and provide oversight throughout the trial.

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Over 250+ members at over 80 sites

SCLRC and our network of 250+ member investigators at over 85 sites have contributed to the research breakthroughs and continuing progress in treating and researching liver disease. The SCLRC network enrolls high volume Phase I-IV clinical hepatology and gastroenterology trials faster than the traditional one-site-at-a-time start-up model.

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Liver

CME Training

SLCRC partners with Scripps Health and the University of Louisville to provide several national CME training series focusing on Hepatitis B and C, NASH, PBC, Chronic and End-Stage Liver Disease.

Services

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Advisory Boards


SCLRC can assist in selecting an Advisory Panel of key opinion leaders to provide input on clinical programs and oversight of the protocol development process, as well as direction and strategy for a clinical trial.

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Clinical Trial Design


SCLRC provides a wealth of expertise in clinical trial development. Our Management team and our consortium Investigators provide strategic insights on trial design and presentations of proposals to the FDA.

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Consistent Research
Guidelines


SCLRC holds Master Agreements with our consortium sites, which includes our standard research guidelines in agreement with ICH guidelines and FDA regulatory requirements in 21 CFR 50.23.

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Continuing Medical
Education Training


In collaboration with Scripps Health and the University of Louisville, SCLRC organizes several national continuing medical education (CME) training series across the country.

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CRO Collaboration

We work so well with Clinical Research Organizations (CROs) because we are not competitors. Sponsors usually include SCLRC in the early stages, so we are often asked to suggest or select a CRO.

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Master Site Agreements

SCLRC Master Agreements are standard across the network and include consistent language for each academic or private medical center.

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PK Facilities

We have sites that accommodate Phase I-IV trials and are equipped to perform 24-hour in-house Pharmacokinetic (PK) testing when required.

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Project Management

Our comprehensive services consist of management of a clinical trial from inception to completion, conception to publication.

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Site Selection

SCLRC has spent over 27 years developing relationships with our sites and tracking enrollment performance. We precisely match Sponsors with sites that will successfully enroll.

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Subject Recruitment

SCLRC provides Sponsors with an accurate representation of enrollment by performing feasibility queries and prudent site selection for each study.

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Sponsor Agreements

SCLRC provides a template of a Master Services Agreement (MSA). Sponsors can elect to use only SCLRC sites or a combination of SCLRC sites and direct contracts.

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Customization

We provide personalized services to best meet the needs of each study. SCLRC is your connection to hand-selected sites to ensure successful, well-executed clinical trials.

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