Sponsor Your Study

Learn more about how ECIR can facilitate the development and management of your clinical trial efficiently and accurately.

Experience Creates Results

The team at ECIR has decades of experience working with nearly every major sponsor across the therapeutic continuum and in all stages of development from discovery through Life Cycle Management. ECIR is honored to have had the opportunity to participate in the education of patients, health care providers, and pharmaceutical company employees around the globe.

Our therapeutic areas of expertise include:

Cardiovascular Disease
Endocrinology and metabolism
Gastroenterology
Nephrology
Dermatology
Medical Devices (Cardiovascular)
Urology
Pulmonology
Plastic and Reconstructive Surgery
Osteoporosis
Ophthalmology
Neurology
Women's Health
Pharmacoeconomics
Allergy

East Coast Institute for Research partners with sponsors to solve a massive problem in clinical trial enrollment

After adopting StudyTeam, the research site network meets or exceeds all enrollment goals set by sponsors

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Our Facilities At Your Service

ECIR conducts research from multiple state-of-the-art research facilities in Northeast Florida and Georgia and has affiliations with several hospitals in the area. Our capabilities encompass Phase II, III and IV clinical trials including both sponsor and investigator initiated studies of drugs and devices.

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Refining Your Clinical Trial Process

ECIR strives for efficiency and accuracy in the clinical trial process. Our diverse, talented and multidisciplinary staff offers customized trial execution regardless of the therapeutic area.

Our investigators are board-certified and our staff is seasoned, making your research experience streamlined and productive. We have investigators and staff with research experience and special interests across the disease continuum. Our research team appreciate the importance of your protocol and the meticulous nature of clinical research, thus our approach is always tailored to your requirements.

Research Services

Board Certified Physicians
Over 20 years of clinical experience
Experienced Certified Clinical Research Coordinators
4 convenient locations throughout Northeast Florida and Georgia
Proven track record of accurate, complete enrollment and high retention
Investigators on-site daily during business hours
Non-academic site utilizing Central IRBs
Secured drug storage at all locations
IATA Certified Staff
Daily access to dry ice
State of the art and thoughtfully appointed exam rooms at all locations
ECG on site
CLIA certified at certain sites
Area for Monitors with refreshments
FedEx, UPS, DSL, and Marken pick-up
Electronic Data Entry capabilities and experience
High speed 24 hour fax on a dedicated line
Comprehensive telephone system with voice mail
24 hour access to on call physician
-70° freezer
-20° freezer on site
Knowledgeable of GCP
Proven history of rapid enrollment
Easily accessible, central location close to freeways, hotels, and airport
HIPAA Compliant

Investigator Initiated Studies (IIS)

At ECIR, we recognize the pivotal role that Investigator-Initiated Studies (IIS) play in drug development and furthering the understanding of current medicines.

For this reason, IIS are a top priority at ECIR. Our team of investigators are constantly developing research proposals that are unique and forward-thinking. IIS are essential to expanding the understanding of medications which are currently approved and in development. Our IIS employ currently approved medications in different ways, including in different patient populations and disease states. We are also exploring new uses for old medications. ECIR, similar to academic institutions, is capable of developing research proposals, presenting the concept to sponsors, preparing a comprehensive protocol, and executing complex clinical studies.

After study completion, ECIR emphasizes dissemination of results, presenting data at key Scientific Congresses and publishing manuscripts in well respected peer-reviewed journals. Our team of specialists and primary care physicians have diverse interests which allow for ECIR to engage in studies that traverse the disease continuum. Our biostatistics program facilitates appropriate study design, accurate data analysis, and ensures the validity of our results.

ECIR provides experienced board-certified investigators and research coordinators in each of the following areas: