PROFESSIONAL STAFF

                                                                                                                           Investigators

Melanie J. Perez, Regulatory Administrator 

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.

Email: mperez@biomedresearchinst.com

Manuel Valladares, Clinical Research Coordinator

Manuel, Cuban doctor (FMD), has over 12 years of experience in the Medical Investigations in Cienfuegos, Cuba. Registered Medical Assistant and Nursing 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 five years.

Email:mvalladares@biomedresearchinst.com

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. 

Email: emendez@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. 

Email: zmartinez@biomedresearchinst.com

Sucel Alvarez, Certified Clinical Research Coordinator

Sucel has five years of experience as a study Coordinator in Clinical Research. She has been responsible for assisting PIs and Senior Staff in coordinating and conducting Federal and/or industry sponsored research studies.Sucel understands IHC, Good Clinical Practice Guidelines, FDA regulations and HIPAA regulations. She is an extremely dedicated worker who has worked eitherindependently or in a group environment. She has strong organizational, communicational and interpersonal skills. Also Sucel has exetensive with EDC systems for ECRF data entry and query resolution, IVRS, data tranfer and central advertisement.  

Email:salvarez@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.

Email: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.

Email: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.

Email:upuentes@biomedresearchinst.com

 

Contact Us

    BioMed

Research Institute

701 NW 57 Ave Ste 220

       Miami, FL 33126

  

Phone: (305) 267-4123

Fax:     (305) 267-4125

E-Fax: (305) 675-6181

Business Hours

Monday through Friday

8:30 AM - 5:00 PM

We are member of the Society for Clinical Research Sites (SCRS)

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