A global network of clinical research sites focused on making your clinical trial a success.

SIMPLIFYING COMPLEXITY. PROVIDING CLARITY.

The Bioclinica Global Site Network simplifies the complexity and solves the challenges associated with clinical trials through a global network of established, readily-available investigative sites. As the preferred provider for many of the largest sponsors, CROs, and biotech companies across the globe, we handle Phase I-Phase IV studies, and are capable of taking a first-in-human drug all the way through to post-marketing.

Our research sites are unified by best-in-class recruitment practices and globalized standard operating procedures (SOPs) and quality systems, yielding the highest quality of data. Each site is staffed by medical experts and trained professionals – therapeutic area specialists, physicians, nurses, study coordinators, raters, and technicians – and has a full array of medical testing equipment.

We bring you more than sites. We bring you a solution.

The Bioclinica Advantage

Through our global network of sites, you are assured:

Fast Delivery

We enroll, care for, and retain high numbers of patients, resulting in faster study completion

Superior Quality

We generate predictable, reliable, world-class data that is inspection-ready

Cost Savings

We enable you to complete studies with fewer sites, reducing the overall time and costs of study delivery

Leverage Bioclinica's Expertise

Why choose a Global Site Network for your clinical trials?

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Bioclinica Global Site Network by the Numbers

30

Dedicated Research Sites

in 14 countries across four continents

15000

Patients Randomized

in the last five years

93

Average

patient retention rate

1

Potential Patients

through databases and patient communities

0

Critical Findings

in sponsor and regulatory audits

Centralized Management & Processes

Our project managers are trained in clinical development and provide a single, central point of contact, visibility into study start up, and ongoing management of clinical site activities.

Centralized Management & Processes

Global Sites

With a geographic spread throughout the U.S., Europe, Latin America, and Asia, we bring you the most diverse standardized global site network in the industry. Each of our investigator sites is:

Structured to optimize the conduct of clinical research
Strategically located to take advantage of access to patient populations
Outfitted with state-of-the-art medical testing equipment
Staffed by physicians, nurses, study coordinators, technicians, and other medical professionals and personnel with therapeutic area specialization

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Leverage Bioclinica's Expertise

Why choose a Global Site Network for your clinical trials?

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Patient Focus

In clinical trials, the patient is the number one priority.

Bioclinica maintains an extensive and dynamic patient database as well as multi-faceted patient communities – all of which can be expertly tapped through our propriety applications and our unique online and social media strategies. We have recruited and managed patients for multiple large studies and can uncover the right patients for your clinical trials rapidly.

Patient Focus

Real-Time Information

Through sophisticated technology, we are able to track the patient’s path all the way through your clinical trial. We will provide you with weekly reports that give excellent visibility into the management of the study at our research sites.

Long-Term Retention

Clinical trials depend on the long-term retention of patients to ensure high-quality data and successful outcomes. You simply cannot afford to have high percentages of patients lost to follow-up. We have extensive experience retaining patients in studies for up to 10 years. Due to the systematic processes and patient-centric care we have in place, more than 90% of the patients we recruit remain active throughout the course of the study.

Best-in-Class Sites

Our sites are capable of managing large volumes of patients efficiently and cost-effectively, increasing patient retention rates. And because our network is unified by globalized standard operating procedures (SOPs) and quality systems, you gain clarity and insight from high-quality, audit-ready data that will drive your trial to a successful outcome.

Specialized Patient Care

Standards of care vary greatly by country, with many patients having no access to quality healthcare treatment. We provide all patients with a general examination that can result in the identification and treatment of problem areas, e.g., blood pressure or renal health. Our staff includes physicians, internal medicine experts, and other specialists to deliver the high level of care patients need. This translates into a positive overall patient experience that yields high rates of patient retention.

Therapeutic Expertise

Extensive capabilities, experience, and expertise to bring clarity to clinical trials.

Over the past two decades, Bioclinica's Global Site Network has delivered outstanding results for Phase 1-4 clinical trials in a multitude of therapeutic areas. We provide:

Qualified patients, having randomized more than 15,000 patients in the last five years alone.
Management and care in our outpatient and inpatient facilities for a successful clinical trial.
Extensive capabilities to perform clinical research and bring clarity to clinical trials and drug development.

Our therapeutic expertise encompasses all the following outpatient indications:

Alopecia
Alzheimer's/AAMI/MCI
Asthma
Cardiovascular
Chronic Constipation
COPD
Device
Dyslipidemia
Endocrinology
Hypertension
IBS
Insomnia

Men's & Women's Health
Migraine
Osteoarthritis
Osteoporosis
Outpatient Oncology
Pain
Restless Legs
Rheumatoid Arthritis
Smoking Cessation
Type II Diabetes
Vaccines
...and more!

Expert People

Everyone on staff at the Global Site Network is committed to clinical research. Therapeutic area specialists, physicians, study nurses, study coordinators, raters, and technicians around the world are highly trained to global standards in order to deliver exceptional service throughout the course of your clinical trial.

Key Opinion Leaders

In addition to our in-house capabilities, we invest in external Key Opinion Leaders (KOLs) to ensure that your research is successful. Our KOLs include:

Craig Curtis, MD, CPI

Key Opinion Leader

Global Site Network

Ira Goodman, MD

Key Opinion Leader

Global Site Network

Roger Bullock, MB.BS, MRCPsych

Key Opinion Leader

Global Site Network

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Want to learn more about Bioclinica’s Lost to Follow-Up (L2FU™) services?

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Exceptional Quality

Standardized, global, validated SOPs support the highest-quality data.

Quality is at the center of all we do. You benefit from our professional Quality Assurance organization, which oversees all operations to confirm the highest-quality data for your study. All sites follow validated SOPs and detailed training programs so that clinical research is conducted to the same high standards of quality and compliance across the globe.

End-to-End Quality

Rigorous compliance. All clinical trial activities are conducted in compliance with ICH/GCP guidelines, the Clinical Trial Directive, relevant local regulations and guidelines, and the clinical trial’s specific requirements.
Local quality control. Every research center has a Local Quality Control unit that reports directly to the Director of Quality Assurance.
Daily quality management. On a day-to-day basis, Central Quality Assurance personnel, in conjunction with Local Quality Control, manage quality at the sites.
Internal audits. A team of Quality Assurance Auditors regularly conducts internal audits as part of our Quality Management System.
Standardized SOPs. All sites follow standardized, global, validated SOPs.

Patient Recruitment & Retention

Uncover and engage the right patients for your clinical trials.

In clinical trials, the patient is the number one priority. That is why we treat every patient with care and respect – from recruitment to trial completion. With global patient databases and over 50 online communities generating more than one million potential patients to draw on, we are able to fill your patient pipeline quickly with fewer sites, saving you both time and money. Our customized marketing programs aid in recruitment and retention, and our proprietary patient engagement tools and strategies drive site performance. And, perhaps most importantly, our staff always treats patients as people – not as projects or as sources of data – keeping retention rates high throughout the course of your study. Sometimes life gets in the way, and patients drop out, along with their valuable data. We also specialize in finding those patients again through our Lost to Follow-Up (L2FU™) service.

94

Overall Success Rate

for patient recruitment and retention programs

200

Completed Programs

with successful results in various therapeutic areas

30

Patient Communities

many of which are the largest in the world for their respective therapeutic areas

We know how to pinpoint the most effective communication channels for your patient group to help you meet or exceed your recruitment goals – on or ahead of schedule and within budget. Bioclinica maintains an extensive and dynamic global patient database and more than 50 multi-faceted online patient communities with over three million unique visitors weekly—all of which can be expertly tapped to rapidly inform, engage, educate, and connect the right patients with your clinical trial.

We seamlessly integrate traditional media approaches with digital strategies that:

Foster expansive patient communities through effective use of social media channels
Reach patients via mobile channels with content that is engaging and shareable
Produce high-quality content that interests and educates readers
Deliver locally-targeted messages to a global network

Clinical trials depend on the long-term retention of patients to ensure high-quality data and successful outcomes. And, patient retention depends on patient engagement. We are experts in the field, retaining patients in studies for up to 10 years and having earned 16 awards for the best-designed patient recruitment and retention materials. We have discovered that the most effective retention strategies begin at the first patient encounter. We customize a program for each study designed to keep patients enrolled until completion, ensuring the study’s statistical power and protecting your investment. Our staff includes physicians, internal medicine experts, and other specialists that deliver the high level of care patients need, providing a positive overall patient experience that yields high rates of patient retention.

Our patient engagement programs include:

Medical symposia and events to educate patients and caregivers
Patient advocacy partnerships to clearly communicate study information to patients and caregivers
Customized print and digital materials to counteract any retention issues that arise

We bring clinical studies delayed due to patient recruitment back on track by detecting hidden recruitment issues, developing an effective recruitment plan, and implementing strategies to restore patient recruitment momentum.

Further, you simply cannot afford to have high percentages of patients lost to follow-up. Although important for study integrity, replacing missing patients delays study timelines and increases study budgets. That’s why we offer our L2FU™ service. We utilize our team’s expertise to customize our search strategies to each study while maintaining patient privacy and transparency through the centralized L2FU portal.

Your sites are where your patients have the greatest interaction with you. Our sites are capable of managing large volumes of patients efficiently and cost-effectively, increasing patient retention rates. And, because our network is unified by globalized standard operating procedures (SOPs) and quality systems, you gain clarity and insight from high-quality, audit-ready data that will drive your trial to a successful outcome. We also offer workshops, support groups, newsletters, and video resources to train your sites in the best practices of patient recruitment and retention.

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Contact us and learn more about finding patients lost to follow-up.

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Post-Approval Research

Post-marketing commitments. New indications. Market extensions. Safety information. Real-world observations. Enhanced formulary positions. Bioclinica can support all your post-approval research requirements and optimize the potential of your FDA-approved drug.

Learn more about our Post-Approval Research Services.

Alzheimer's/AAMI/MCI

At Bioclinica, we have worked for decades with patients at every stage of Alzheimer's disease and cognitive impairment. Our facilities have been designed with the size and infrastructure required to conduct large prescreening programs and to execute the protocols of prodromal Alzheimer's disease/mild cognitive impairment clinical trials.