Tranquil Clinical Research
Joshua Davis, B.A., is a Clinical Research Quality Assurance Analyst at Houston Methodist, responsible for ensuring GCP compliance and developing educational content for various clinical research programs. In addition, Joshua serves as a Clinical Research & Regulatory Affairs Associate at Tranquil Clinical Research and Consulting Services, focusing on study initiation and regulatory compliance. Previous roles include Community Outreach Lead at Ascend Behavior Partners and Clinical Outreach Coordinator at Texas Children's Hospital, where Joshua maintained patient engagement and regulatory adherence. With experience in quality assurance and medication management at organizations like QuVa Pharma, MD Anderson Cancer Center, and Behavioral Hospital of Bellaire, Joshua has a strong background in clinical research and pharmaceutical oversight. Currently pursuing a Master of Science in Clinical Mental Health Counseling, Joshua holds a Bachelor of Arts in Health Communication from the University of Houston-Downtown and an Associate of Arts in Communication from College of the Mainland.
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Tranquil Clinical Research
Tranquil's ultimate goal is excellence in the clinical trial process and bringing trustworthy products to patients. Tranquil clinical research was created to ensure that the entire clinical trial, device, and drug development process is conducted with ethics and the patient in mind first and always. The business model ensures a clients drug, device or investigational product in the clinical trial is adherent to the highest level of quality and integrity in the services we provide.