Inquest Clinical Research is a dedicated full-time research organization focused on providing high quality standards in clinical research. Our facility occupies 2000 sq. ft. of space in the Baytown Medical Center area near the world renowned Texas Medical Center. We currently have a database of over 20,000 patients with different demographics in the cosmopolitan city of Houston. Our data is compliant with 21 CFR, HIPAA, and Privacy Act.
Inquest Clinical Research employs a staff of 7 full-time trained clinical coordinators that are dedicated to the mission and vision of the organization. They coordinate clinical patient care ensuring that the patient’s health, safety, and well-being are protected at all times.
The recruitment and marketing department is staffed by a full-time recruiter who has developed and established dynamic market bases and resources to maintain current patients and recruit new ones to participate in clinical research. Patient recruitment efforts are targeted via radio/RV advertisements, newspapers, mailers, patient databases, health fairs, patient referrals, word of mouth referrals, physician referrals, and sponsor referrals. Recruiters are knowledgeable and trained in subject protocol eligibility requirements for each study to pre-screen, pre-qualify, and schedule potential research subjects during the initial phone screening for participation.
We have a database of 50,000 patients with different demographics in the cosmopolitan city of Houston. Our datadase is compliant with 21 CFR, HIPAA, and Privacy Act. We have a database for all indications in specialities like Internal Medicine/Family Medicine, Cardiology, Gastroenterology, Psychiatry, Rheumatology, Dermatology, and Hematology.
Inquest Clinical Research contracts with 6 Principal Investigators; 1 Internist, 1 Family Practice, 1 Cardiologist, 1 Gastroenterologist, 1 Psychiatrist, and 1 Ophthalmologist. All are licensed physicians who are experienced, highly trained, and knowledgeable in clinical research and GCP/ICH guidelines. They oversee the overall process of the research activities and ensure that they are carried out in accordance with the respective clinical protocols.
The regulatory department at Inquest Clinical Research employs a full-time professional who specializes in processing any and all regulatory documents necessary to ensure complete IRB compliance standards.
Inquest Clinical Research employs a full-time licensed phlebotomist. A CLIA waiver is also in place at the facility.
Inquest Clinical Research employs a full-time on-site auditor/QA professional so that we may deliver high quality clean data consistently. We will ensure that the study site is adhering to good clinical practices and complying with all restrictions on the handling and the usage of the investigational drugs as specified by each study.
Monitor office space is set aside for monitor visits from one to three days use if necessary. Inquest Clinical Research has two dedicated monitor offices available to accommodate monitor visits. Both offices include phone, printer, fax, and high-speed internet capabilities.
Business Developer & Quality Assurance
Business Developer & Recruitment
FOR MORE INFORMATION, CALL US AT (832) 606-2053
Inquest Clinical Research, LLC was created by a group of healthcare professionals with a vast range of experience and expertise in conducting clinical drug research.
1690 W. Baker Road Baytown, TX 77521
+1 (832) 606-2053