One-Stop CRO for Global Clinical Trials Full Services Clinical Research Organization for Phase I-IV Clinical Trials
in the United States, Europe, United Kingdom, Aisa-Pacific,
Middle East, North Africa, and Latin America
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CRO Services

Clinvigilant supports biotech, pharmaceutical and medical device companies with tailored clinical Operation Services. We combine the full-service capabilities and global reach of a large CRO with the flexibility and personal approach only a mid-size CRO can deliver. With Clinvigilant you get a shared commitment to your success. Expect more.

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project Management

Clinvigilant Research provides skilled project managers that are well suited to the needs of clinical trials. With an average tenure of 10+ years in the industry…
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Data Management

Our databases fulfill important baseline attributes while allowing for the specialized configuration required for regulatory report outputs, and are configured with…
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Our biostatistical staff members provide more than data analysis; they have in-depth knowledge of the methods for studying and the techniques that are used…
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Clinvigilant Research monitors have experience with both outpatient and inpatient records and procedure notes. Monitors are also trained in control response…
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Our Expertise

Clinvigilant demonstrates scientific and medical excellence across a broad therapeutic spectrum with industry-leading capabilities in the following areas:


Hematology and Oncology

Nearly 10,000 patients across 800 partners sites in the last 5 years

Dematology, Immunology & Inflammatory Diseases

A global network of 9,000 sites and our own in-house experts and clinic


Specialized senior expertise and global advisors complemented by 600 partner sites

Internal Medicine

12,000 partner sites and nearly 2,000 projects in the last 5 years


More than 300 full-services clinical studies across neurology, psychiatry, and pain indications

Autoimmune Diseases

Experienced medical leadership with a thorough understanding of the complex conditions that cause autoimmune diseases.


Effectively plan, conduct, and integrate your cardiovascular and cardiac safety trials regardless of trial size or safety demands.

Endocrine and Metabolic

Unrivaled in this space, Medpace can help navigate the complexities and regulatory scrutiny of endocrine and metabolic development programs.

Infectious Diseases and Vaccines

Broad experience designing and conducting global clinical trials in antivirals, antibacterials, antifungals and vaccines.

NASH & Liver Disease Clinical Development

As an experienced leader in this space, we help sponsors gain a competitive edge for NASH/NAFLD clinical trials.

Nephrology and Renal Disease

Strategic leadership to design and execute your nephrology trials supported by our dedicated renal experts and considerable experience.


Strong track record for recruiting pediatric populations while maintaining ethical considerations at a local and global level.

Rare Disease & Orphan Indications

Global expertise in enrolling patients while maximizing site selection to create realistic study feasibility.

Cellular and Gene Therapy

Specialized leadership team with hands-on and in-depth experience in the specific requirements of advanced therapies.

Radiation Therapy

Our radiation group has proven expertise in radiation oncology, radiation device, and radiopharmaceutical clinical trials.

Our Experience


Clinical Trials - Data Management


Regulatory Submission


Regulatory Inspection


satisfied customers

Our client's testimonials