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.
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.
To advance science and patient care with innovative, high quality and ethical clinical research.
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.
Our staff has more than 35 years combined experience conducting clinical trials. Our staff is fluent in both English and Spanish.
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.
I am employed at the 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.
I have worked in research for six 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 four years before I earned my way up to conducting studies as a Clinical Research Coordinator with SFCRI. I started working for SFCRI 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.
