MEET OUR PRINCIPAL INVESTIGATOR:
Dr. Farshid Etaee, MD
Principal Investigator | Physician-Scientist | Medical Director | Interventional Vein Specialist
Dr. Farshid Etaee is a board-certified physician and accomplished clinical researcher with expertise in Interventional Vein Therapy, Aesthetic Medicine, Internal Medicine, and Clinical Trial Leadership. He currently serves as Principal Investigator, Medical Director, and Adjunct Faculty, blending academic excellence with hands-on clinical experience.
His research journey began at the Neurophysiology Research Center at Hamadan University in Iran, followed by postdoctoral fellowships in cardiovascular medicine at leading institutions including the University of Kentucky and UT Southwestern. He contributed to numerous studies in dementia, addiction, anxiety, cardiovascular disease, dermatology, and aesthetic medicine, and expanded his research during residency at Yale New Haven Health, where he also served on Yale’s IRB as a scientist member and the New Haven County Medical Association Board of Governors.
Before founding this center, Dr. Etaee led and supported over 35 clinical trials at two major research centers in California. He has published 65+ papers with over 10,000 citations, presented at 35+ global conferences, and serves on editorial boards for several journals. Dr. Etaee’s Google Scholar Profile (Google Scholar profile) showcases his broad scientific impact.
Currently, Dr. Etaee practices as an Interventional Vein Specialist at VIP Medical Group and serves as Adjunct Faculty at the American Canadian School of Medicine. His leadership in both research and clinical care reflects a deep commitment to advancing medicine through high-quality, patient-centered clinical trials.
BUSINESS DEVELOPMENT & OPERATIONS
Chris Sauber
Chris Sauber’s journey in the clinical research field has been diverse and extensive. Starting as a Clinical Research Coordinator (CRC), he developed a foundational understanding of clinical trials, patient care, and data management. His dedication and expertise led him to roles with increasing responsibility, such as Site Director and ultimately Site Owner, where he managed entire research sites, overseeing both administrative and clinical operations.
Recognizing a need in the industry, Chris transitioned into consulting. He now leverages his broad experience to help others establish and optimize their research sites. His consulting work includes advising on regulatory compliance, operational efficiencies, and strategic planning, ensuring new site owners are well-prepared to navigate the complexities of clinical research.
In addition to site establishment, Chris occasionally advises Contract Research Organizations (CROs) and Sponsors on their clinical research needs. His insights help streamline study designs, improve patient recruitment strategies, and enhance overall study management processes.
Chris’s multifaceted career also includes roles as a Clinical Research Associate (CRA), where he monitored trial progress and ensured adherence to protocols; an auditor, where he evaluated compliance and data integrity; a consultant, providing tailored advice to various stakeholders; and a project manager, coordinating large-scale clinical trials and ensuring successful outcomes.
This breadth of experience allows Chris to offer a holistic perspective on clinical research, making him a valuable asset to any organization seeking to excel in this field.