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.

Efren Mendez Castilla

Clinical Research Coordinator

Efren, Cuban doctor (FMD), graduated at University of Medical Sciences of Havana,  has over 5 years of experience in medical investigations. Registered Medical Assistant. 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 three years.

emendez@biomedresearchinst.com

Melanie J. Perez

Clinical Research Coordinator

Melanie has been working at BioMed for the past 4 years as our Regulatory Administrator and Study Coordinator. She has been responsible for all regulatory work in research studies, and assisted PI’s and the senior staff in coordinating, and additionally as a main 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 2 years of experience working as a Study Coordinator in research studies. Qualified in EDC systems for ECRF data entry and query resolutions, knowledgeable in laboratory work, and has assisted with regulatory 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

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

Ileana Hernandez

Medical Assistant / Phlebotomist 

Info to be updated.

ihernandez@biomedresearchinst.com

Raul Eris 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

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

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