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Divya Chauhan

Clinical Research Coordinator at Arizona Arthritis and Rheumatology Research, PLLC

Divya Chauhan is a Clinical Research Coordinator at Arizona Arthritis and Rheumatology Research, PLLC since December 2022. Previously, Divya held roles including Global Health Intern at Esperança, contributing to data collection tools and program management, and involvement in the Mayo Alix School of Medicine Pre-medical Scholars Program. As an Undergraduate Research Assistant with the Learning Health Systems Project, Divya focused on COVID-19 strategies for indigenous peoples. Leadership as Clinical Branch Leader in the Refugee Education and Clinic Team involved establishing health resources for refugee populations and overseeing clinical operations. Divya's educational background includes Bachelor's degrees in Biological Sciences and Justice Studies from Arizona State University.

Location

Gilbert, United States

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Arizona Arthritis and Rheumatology Research, PLLC

Arizona Arthritis & Rheumatology Research (AARR) remains at the forefront of rheumatologic care by participating in clinical trials of new rheumatologic drugs and the enrollment and supervision of patients who qualify and who may be in need of other potentially effective therapies. In a clinical drug trial, medications are supplied at no cost to participating patients. Clinical trials may offer benefit to patients who have not responded to conventionally available treatments. As the research wing of Arizona Arthritis & Rheumatology Associates (AARA), we keep involved in the valuable process of new drug development. As long as people continue to suffer from the damage of immunologic illness and musculoskeletal disorders, medical scientists and pharmaceutical and device companies will forge ahead for the next advancement in treatment. Only real people with these disorders can move this science ahead for themselves and others who may suffer these disorders in the future. We encourage our patients whenever appropriate to consider contributing to medical science through enrollment in FDA supervised clinical trials.


Employees

11-50

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