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Bioclinica is a specialty clinical trial services provider that accelerates the development of new medical therapies.

Clinical trials are a complex undertaking. While there are many companies available to support trials, many offer a monolithic approach—one that is massive, indivisible, and rigid. These methods tend to focus on the system and not on your needs.

Bioclinica puts your objectives first. We understand that the fundamental purpose of a clinical trial is to discover the truth. The ability to see key details and uncover hidden insights will help you find the truth quickly and efficiently.

That's why Bioclinica has built an expert, multifaceted organization that brings clarity to clinical trials. We help you see more clearly, so you can make better decisions.

Strong Sites

providing high-quality data and superior patient recruitment and retention methods

Agile Technology

systems and domain expertise to reveal data insights and speed drug development

Scientific Experts

who can see more deeply into biomarker data and identify things others might miss

Clients Includes Top 100 Pharma & Top 10 CROs
Drugs Approved by the FDA Using Imaging and Biomarkers
Clinical Trials Supported
Employees Worldwide
Years of Experience

Bioclinica Solves Critical Pain Points For Trial Sponsors and CROs

Bioclinica leverages its therapeutic and clinical expertise, technology, data analytics and deep customer experience to solve key industry challenges. By bringing together key functional areas of clinical trial support, Bioclinica solves a variety of critical pain points that can hinder clinical trials.

Clinical development process is long and expensive

Solution: Reduce time to market, decrease the number of patients required, improve measurement precision, and enhance sponsor ability to identify efficacy and safety earlier in a trial

Clinical trial imaging is non-standardized and complex

Solution: Train and qualify trial sites to ensure data standardization; navigate logistics of digitally collecting, processing, and storing images from multi-country trials across dozens or hundreds of sites

Paper-based processes and legacy software are inefficient

Solution: Software solutions accelerate data collection, analysis, and feedback from clinical trials. Investigator payment solution eliminates payer errors and streamlines payment process globally

Recruitment is #1 cause of trial delays

Solution: A multifaceted "patient engagement" approach employing digital marketing strategies, patient communities, and databases accelerates recruitment and improves retention

Regulations and surveillance related to adverse events

Solution: High-quality safety case management and regulatory submission services utilizing cost effective resources and technology solutions

Large investigator site networks are inefficient

Solution: Site network provides local knowledge, physician access, and an extensive patient database, yielding rapid access to large eligible patient populations and improved retention rates

More About Bioclinica


A dedicated team of clinical trial experts with years of experience.


Want to change the future of clinical trials? This is the place.


With offices in North America, Europe, and Asia, our company is global but service is local.


Giving back to the communities where we do business.


Leader in Clinical Trial
Management Solutions

Bioclinica is organized into three business segments so that we can provide expert service and multifaceted technologies. Our Medical Imaging & Biomarkers segment includes an Imaging Core Lab, a Cardiovascular Safety division, and a Molecular Marker Laboratory. Our eHealth segment comprises eClinical Solutions, Randomization & Trial Supply Management, Safety & Regulatory Solutions, and Financial Lifecycle Solutions. Under the Global Clinical Research segment, we offer a network of research sites, patient recruitment, and a Post-Approval Research division.
bioclinica (16 hours ago)
RT @Xtalks: When is Central Imaging Needed in #ClinicalTrials? @bioclinica
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RT @phillytechnews: 11/7: BioClinica, USA Technologies buy California firms ; First Round names female general partner…
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RT @eClinical_Jen: Content from the FDA Webinar on Study Data Technical Conformance Guidelines is here: #ITTX17
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RT @CenterWatch: .@US_FDA approves first #digital pill with sensor to track #patients adherence,
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RT @RAPSorg: Could you use a mid-week laugh? Many #regulatory pros will appreciate this one, courtesy of @CharlesTam
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Latest Blogs:

Removing Risk from Clinical Trial Management System (CTMS) Implementations
Collaboration Between Clinical Operations and the Logistics and Supply Chain Teams is Key to Trial Success
The Value of Protocol Review
CTMS and RBM: Hot Topics at OCT Nordics in Copenhagen
Congressman Meehan and Bioclinica CEO John Hubbard at recent visit to Bioclinica's Audubon offices