Becky has been working in healthcare for 30 years, and has been at CMR for 15 years. In those 15 years, she has worked on over 250 trials in psychiatry, pain, and addiction. Before working at CMR, Becky worked in surgery and recovery rooms.
H. Mikel Thomas, M.D.
Chief Scientific Officer
Dr. Thomas is a board-certified Adult and Addiction Psychiatrist with 30 years of experience. He completed medical school at Texas A&M Health Science Center College of Medicine, psychiatry residency at the University of Kansas School of Medicine, and psychiatry residency/fellowship at Yale School of Medicine. Throughout his career, he has advised over 300 studies on depression, migraines, PTSD, ADHD, and many others.
Vishal Adma, M.D.
Dr. Adma is a board-certified Psychiatrist and physician executive. He completed psychiatric residency at the University of Kansas Medical Center, a Master’s in Nutrition and Food Management from the University of Central Oklahoma, Certification in Medical Quality from the American Board of Medical Quality, and Certification as a Physician Executive through American College of Physician Executives.
Kiesha, a clinical coordinator who specializes in patient recruitment, joined CMR two years ago. Throughout her 12 year career in healthcare, she has worked as clinical coordinator and as a Lab Technician at St. Luke’s Hospital. While at CMR, she has coordinated PTSD, migraine, and ADHD trials.
Christine Lambeth, LPN
Christy, our study coordinator, has worked at CMR for 10 years, and has 30 years of experience working in research. Before CMR, she received her LPN from KCKCC and worked as a research assistant at PRA and Radiant Research. Christy currently works on the binge eating trial and oversees various other trials.
Director of Regulatory Affairs
Andrew has worked at CMR and in healthcare for three years. Before working in regulatory, Andrew coordinated social media. He graduated from Northwest Missouri State University with a BS in public relations, and now has an ACRP-CP certification.
EDC Manager/Regulatory Affairs Coordinator
Abby has been at CMR for five years now. Before switching to regulatory affairs, she was a clinical coordinator. She graduated from Wichita State University and over her last 15 years in healthcare, she has worked on many Allergan and migraine trials. Before working at CMR, she was a clinical coordinator at an outpatient lab.
Kayla has seven years of experience in healthcare and one year at CMR. She previously worked at University of Kansas Health System as well as the Center for Pharmaceutical Research. In the past, she assisted on vaccine and migraine trials, and currently coordinates migraine and depression trials.
Rachel, our clinical coordinator for studies on Fibromyalgia and Stuttering, obtained her Bachelor of Arts from Life Pacific College. She then spent 12 years working as a Patient Care Technician, Lab Technician, and Lab Coordinator before coming to CMR two years ago.
Lindsay has been a clinical coordinator at CMR for two years. Before CMR, she spent seven years working as a research coordinator and medical assistant. Lindsay has IATA, BLS, RMA, CMA, and CNA certifications from Johnson County Community College, Wright Career College, and an Associates of Applied Science. She has worked on trials for depression, anxiety, OCD, migraine, and various pain trials.