Clinical Research Services
Phase I | Phases II | Sponsors | Experience
Investigators | Specialities

Phase I Specialists (State-of-the-Art Research Center)

Phase II through Phase IV Specialists (Research Center Capabilities and Private Practice Setting Capabilities)
Gulf Coast Research LLC has two offices in Louisiana. We contract with pharmaceutical companies (Sponsors) and Contract Research Organizations (CROs) to recruit, coordinate, and manage Phase I through Phase IV clinical trials throughout our vast and diverse network of Clinical Investigators in South Central Louisiana.

Our highly efficient Research Center structure allows us to respond quickly to the Sponsor's research needs. Our centralized management and coordination system produces streamlined and rapid study start-up. We utilize experienced Board Certified Investigators in all medical specialties to recruit patient volunteers and perform Phase I though IV clinical trials.

We have a very experienced regulatory manager, Linda Babin, who handles the coordinating of all regulatory documents at study initiation and throughout the term of each protocol along with the assistance of each lead coordinator to ensure the quickest turnaround of documents for each protocol.

Working with Pharmaceutical Companies (Sponsors & CROs):
Gulf Coast Research works closely with study Sponsors and CROs to understand all aspects of each study we contract to work on. Gulf Coast Research works very closely with our Network of Investigators to recruit, enroll, and schedule volunteers to participate in the studies.

All contracts/budgets, regulatory/IRB, and study specific paperwork is prepared by our key departments while each coordinator prepares source documents and recruitment plans along with each investigator to ensure quick study start up and the greatest potential for success for each protocol. Gulf Coast Research ensures that each study follows strict GCP guidelines and adheres to Study Protocol in order to produce high quality unbiased study data for our Sponsors. All GCR personnel receive training in GCP guidelines, protection of human subjects, IATA certification for laboratory processing and shipping, and company SOPs before working on any clinical trial.

Experience:
Gulf Coast Research LLC has worked on over 200 successful Phase I through Phase IV clinical trials since the year 2000. Some of the Sponsors and CROs we have worked with are mentioned below:

Pfizer
GSK
Proctor & Gamble
Merck
Baselia
Johnson & Johnson
AstraZeneca
TAP Pharm.
Ortho McNeil
Advanced Biologics
Theravance
Luitpold
Vertex
Abbott
Boehringer Ingelheim
Xanodyne
Purdue
DuraMed
Bristol Myers Squibb
PRA Int.
Omnicare
Novum
I3 Research
Duke Clinical Research
Wyeth Pharm.
Axcan
Altana
Kyowa Pharm
PPD
Sankyo
Aventis
Schwarz Pharma.
Sucampo
Xenoport
Zymo Genetics

Extensive Network of Investigators:

Allergy & Immunology
Internal Medicine
Pain Control
Cardiology
Neurology
Pediatrics
Dermatology
Obstetrics & Gynecology
Pulmonology
Endocrinology
Ophthalmology
Rheumatology
Family Medicine
Oncology
Sleep Medicine
Gastroenterology
Orthopedics
Surgery
Infectious Disease
Otorhinolaryngology
Therapeutic Specialties

Specialties We Have Excelled In and Exceeded Recruitment Goals:

RLS
Complicated Skin and Soft Tissue Infections
Arthritis Pain
General Pain
Women’s Health (Low Sex Drive and Birth Control Hormone Therapy)
Dermatology
Infectious Disease
Gastroenterology



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