SFCRI: Who We Are

South Florida Clinical Research Institute is a multi-specialty clinical research firm that provides facilities and services to advance patient care through pharmaceuticals or medical devices.

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SFCRI’s Mission

To advance science and patient care with innovative, high quality and ethical clinical research.

Our Partners

We partner with Principal Investigators to explore cutting edge clinical research and pursue new treatment options.


An ethical and professional environment. Delivery of efficient, timely sponsor data. Patient recruitment and retention. Lower labor costs. The option for specific in office research activities.

Meet SFCRI’s Team

Our staff has more than 35 years combined experience conducting clinical trials. Our staff is fluent in both English and Spanish.

LeRoy Reynolds, RPh
Clinical Operations Officer

With 29+ years of Pharmaceutical Experience, I consider myself a veteran in Clinical Research affairs. Before managing operations here at SFCRI, I worked 29+ years as the Regional Research Manager for the Southeastern United States for Eli Lilly and Company.

My responsibilities encompassed Sales & Marketing and Medical & Clinical Operations. They tasked me with providing operational expertise to customers through ownership of the site performance from site selection through site closeout. I Identified and selected high performing investigator sites that regularly executed trials with high quality and cost-effective speeds, and developed and managed institutional and key investigator relationships within my region, by serving as the primary interface between Lilly, the investigator, and the vendor representatives to ensure a successful Clinical Trial.

These skills are now used to ensure that South Florida Clinical Research Institute is successful in the following key areas:

Business Management – ensuring timely data delivery and integrity alongside meeting clinical trial milestones for our sponsor partner.

Business Development – screen, test and develop investigators for clinical trial participation.

Communication/Information Management- implement technology to ensure good quality data to the CRO/Sponsor.

Compliance – hold all site personnel accountable for inspection readiness throughout the trial and to support regulatory inspections.

Dr. Ivonne Reynolds, D.O.

A board-certified obstetrician and gynecologist and fellow of the American College of Osteopathic Obstetricians and Gynecologists, Dr. Reynolds has more than 25 years of experience in women’s health. She combines deep medical expertise with an ability to build relatable, trusting relationships with her patients – ultimately ensuring outstanding obstetric and gynecological care.  Dr. Reynolds is the Medical Director and Principal Investigator for 10 plus years across multiple therapeutic areas such as women’s health, cardiology, diabetes and men’s health.  She has conducted over 33 trials.

Veronica Hibbert
Clinical Research Coordinator

I am employed at South Florida Clinical Research Institute in Margate, Florida as a Clinical Research Coordinator (CRC). I perform various activities related to medical research but particularly Clinical Trials. Furthermore, as a Clinical Research Coordinator, I monitor and handle patient safety and manage data integrity issues associated with Clinical Research studies. I am also responsible for ensuring that all of the clinical research is conducted in accordance with the approved and appropriate protocol, such as Standard Operating Procedures, ICH guidelines, and other regulatory requirements.

Tracy Milgram-Posner
Business Development

I am a seasoned business executive with 20+ years of pharmaceutical sales and marketing and operations management experience in the medical sector. Recognized for demonstrating a natural aptitude for launching businesses with a mission, as well as for expanding successful organizations, I have a history of contributing to company growth throughout my career.

I am the Founder of BRCA Strong where I built an organization to support women enduring preemptive mastectomies or hysterectomies. I provide support and resources to women and develop a doctoral panel to continually update the material. I liaise with senior leadership, stakeholders, and clients to ensure the company’s support structure is empowering and inspiring its clientele.

Dr. Jessica White, D.O.

A board-certified obstetrician and gynecologist, Dr. White has nearly 10 years of experience in women’s health. Highly respected by her patients, Dr. White is known for her accessibility and for building open, trusting relationships, holding what her patients say in high regard. Her ability to build a personal connection keeps the lines of patient communication open, which often leads to catching and addressing healthcare issues early on. Dr. White is a Sub Investigator for 4 years across multiple therapeutic areas such as women’s health, cardiology, diabetes and men’s health.

Dr. Juan Loy, MD
Principal Investigator Internal Medicine

Dr. Juan Loy is an internist in Margate, Florida and is affiliated with Northwest Medical Center-Margate. He received his medical degree from Santiago University of Technology School of Medicine and has been in practice for more than 20 years. Dr. Loy has been a Principal Investigator for 6 years across multiple therapeutic areas such as women’s health, cardiology, diabetes, and men’s health.

Ana Ochoa
Clinical Research Coordinator

I have worked in Research for 6 years and had the chance to understand Research from the inside out, learning from a solid foundation with support from Research professionals with many years of experience and a solid understanding of the basics of the clinical science of Research. I worked as a Research Assistant for 4 years before I earned my way up to conducting studies as a Clinical Research Coordinator with SFCR. I started working for SFCR in 2018 and am thrilled to keep working alongside such a great group of professionals. With my experience in Research and my continuous learning ambition, I thrive to deliver only the best medical care and safety to our patients. Keeping excellence in our data collection procedures and integrity is my top priority when conducting Clinical Trials. I believe that understanding patient care and linking that to delivering a great experience to our Research subjects while keeping a sense of quality and ownership in the way we do Research is the difference-maker in today’s market.

Dr. Farah Eghlim-Irani, PhD
Clinical Project Manager
A Certified Quality Auditor and Fellow of the National Academy of Clinical Biochemistry, Dr. Irani has more than 15 yrs of experience in research and clinical trials. She combines her quality expertise and training in Six Sigma Black Belt to manage clinical projects.
Dr. Zeeshan A. Mahmood, D.O.

Dr. Zeeshan A. Mahmood, D.O., is board certified in family practice. He graduated from Nova Southeastern University Medical School in Fort Lauderdale, FL. Upon completion of his medical school he entered into residency training in Orlando, FL. He has focused his education and experience on family medicine and urgent care. Being a native Floridian, he was excited to complete both his education and residency locally. He currently resides in Coral Springs, FL. Dr. Mahmood is an avid sports fan who enjoys playing various sports and supporting the local teams.

Dr. Nashay Clemetson, MD
Board Certified Dermatologist

Dr. Nashay Clemetson, MD is a board-certified dermatologist. Trained at top institutions in her field – Johns Hopkins University and the University of Miami—Dr. Clemetson has a special interest in treating skin of color and hair loss. She values spending quality time with and providing accessible, affordable, high-quality care to her patients. For these reasons, she chose the direct care model for her practice. Dr. Clemetson recently served as an assistant professor and was the first Ethnic Skin Fellow in Dermatology at the Johns Hopkins University, where she honed her skills in treating skin of color. She is a Diplomate of the American Board of Dermatology, a Fellow in the American Academy of Dermatology, and an Associate in the Skin of Color Society. A native of Jamaica, she recently returned to South Florida, where she lives with her family.

Jeanie Bonhomme
Research Assistant
Dr. Chrissy Williams-Coleman, MD, MS

I am a medical doctor who is passionate about patient care, research, and the medical sciences. I’ve worked on pre-clinical studies while serving as a researcher in a tumor immunology lab. I’ve also worked in various medical environments including internal and family medicine practices where I was privileged to assist in the care of individuals with varying acute and chronic conditions. I desire to carry over my medical knowledge, patient care skills, and research experience into the clinical trial setting, contributing to the development of better treatment options for patients. I make every effort to conduct my research with integrity and high ethical standards, adhering to GCP guidelines and placing patients first. I enjoy contributing to the advancement of scientific knowledge through these efforts.

Dr. Vivian Rose

Dr. Vivian Rose is a distinguished Endocrinologist specializing in the treatment of disorders related to hormone-secreting glands, which play a crucial role in regulating various bodily functions. With a passion for improving patient health and well-being, Dr. Rose focuses on a wide range of endocrine conditions, including diabetes, thyroid disorders, metabolic and nutritional issues, pituitary diseases, and concerns related to menstrual and sexual health. Dr. Rose’s journey in the field of endocrinology has been nothing short of remarkable. Just six months after becoming a referring physician, his dedication and expertise led them to take on the role of Principal Investigator. This demonstrates his commitment to advancing the understanding of endocrine disorders and seeking innovative solutions for the benefit of patients. Dr. Rose’s work as a Principal Investigator is a testament to his relentless pursuit of knowledge and his dedication to the betterment of healthcare in the field of endocrinology.

Dr. Kalvin D. Cline, DHSc, MS
Head of Business Development

Work with us:

  • Coordination of clinical trials according to FDA, ICH and GCP guidelines
  • An ethical and professional environment
  • Delivery of efficient, timely sponsor data
  • Patient recruitment and retention
  • Lower labor costs
  • The option for specific in office research activities
Learn More About Becoming a Principal Investigator