Our company has experienced personal in research and clinical care. All our personnel have been trained in FDA Regulations, GCP, Site management and Good Documentation Practices.
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Dr. Guido A Perez
Investigator / Owner
Dr. Perez is a co-founder of BioMed Research Institute. He has over 25 years of experience as a physician. He worked in Havana, Cuba as an Internist for 10 years. He has worked as a Medical Doctor in Miami, FL since 1999. He has more than 15 years of experience as a Principal Investigator and Principal Investigator in several therapeutic areas. He took the 12th Annual Clinical Research training for physicians at University of North Florida. Jacksonville, FL.
gperez@biomedresearchinst.com
Ileana Puentes
Finance Director / Owner
Ileana is a co-founder of BioMed Research Institute. She has extensive experience in leadership, strategic decision making, and public relations and as financial expert analyzing and presenting financial reports accurately. She attended the course “Introduction to Clinical Research, 120 Hours training Program including the following topics: Drug research and development process, FDA Code of Federal Regulations; Good Clinical Practice and International Conference of Harmonization and Study Coordinator responsibilities.
ipuentes@biomedresearchinst.com
Manny Garcia
Regulatory Administrator
Manny has been working at BioMed for the past 2 years as our Regulatory Administrator. He has been responsible for all regulatory work in research studies, and assisted PI’s and the senior staff. He attended the course “Introduction to Clinical Research, 120 Hours Training Program which included the following topics: Drug research and development process, FDA Code of Federal Regulations; Good Clinical Practice and International Conference of Harmonization and Study Coordinator responsibilities.
mgarcia@biomedresearchinst.com
Efren Mendez Castilla
Foreign Medical Doctor /
Clinical Research Coordinator
Efren is a Cuban doctor (FMD), graduated at University of Medical Sciences of Havana with over 10 years of experience in medical investigations. Registered Medical Assistant. He has been responsible for assisted PI’s as a Main Study Coordinator. He attended the course “Introduction to Clinical Research, 120 Hours Training Program including the following topics: Drug research and development process, FDA Code of Federal Regulations; Good Clinical Practice and International Conference of Harmonization and Study Coordinator responsibilities. He has worked as a Clinical Research Coordinator for seven years.
emendez@biomedresearchinst.com
Melanie J. Perez
Clinical Research Coordinator
Melanie has been working at BioMed for the past five years as our Regulatory Administrator and now as Study Coordinator. A current student in Florida International University, she’s pursuing a degree in Biological Science to one day attend a Medical School Program. She attended the course “Introduction to Clinical Research, 120 Hours Training Program which included the following topics: Drug research and development process, FDA Code of Federal Regulations; Good Clinical Practice and International Conference of Harmonization and Study Coordinator responsibilities.
mperez@biomedresearchinst.com
Zaida Martinez
Clinical Research Coordinator
Zaida has over 5 years of experience working as a Study Coordinator in research studies. Qualified in EDC systems for ECRF data entry and query resolutions and knowledgeable in laboratory work. She is a dedicated worker and prioritizes patient care. She attended the course “Introduction to Clinical Research, 120 Hours Training Program which included the following topics: Drug research and development process, FDA Code of Federal Regulations; Good Clinical Practice and International Conference of Harmonization and Study Coordinator responsibilities.
zmartinez@biomedresearchinst.com
Ileana Hernandez
Foreign Medical Doctor / Laboratory
Ileana is a Cuban doctor (FMD), graduated at University of Medical Sciences of Havana with over 10 years of experience as Certified Medical Assistant. He has been responsible for all Laboratory work on site. She attended the course “Introduction to Clinical Research, 120 Hours Training Program including the following topics: Drug research and development process, FDA Code of Federal Regulations; Good Clinical Practice and International Conference of Harmonization and Study Coordinator responsibilities.
ihernandez@biomedresearchinst.com
Ulises Puentes
Business Development / Owner
Ulises is a co-founder of BioMed Research Institute. He has experience in marketing, business development strategies, He attended the course “Introduction to Clinical Research, 120 Hours training Program including the following topics: Drug research and development process, FDA Code of Federal Regulations; Good Clinical Practice and International Conference of Harmonization and Study Coordinator responsibilities.
upuentes@biomedresearchinst.com
Raul Erick Mederos
Software Development
15 years of experience in Software Development with the most modern programming techniques. Including analysis, designing and implementing information applications, service oriented, with multiple layers and using design patterns. Proven track record utilizing Microsoft and Java technologies to implement enterprise solution Strong Knowledge of information Systems Architecture, Object Oriented Design principles, Database Design and the Software Development Methodologies.
rmederos@biomedresearchinst.com