STAFF
Clinical Pharmacology of Miami, Inc has principals and personnel with many years of history and experience working together. Our staff have diverse specialized educations and skills suited to working at CPMI and performing exceptional clinical research studies. From concept to completion, the collective efforts of our staff will be an asset and a scientific resource you can add to your team. Many of our key personnel have worked under the direction and supervision of the CPMI principals for many years and will continue to do so.
Our staff members are:
• Loyal and dedicated
• Board certified physicians, nurse practitioners and physicians assistants
• Certified or registered, experienced clinical research coordinators and technicians
• ACLS and BLS certified
• GCP/ICH trained and certified
• OSHA trained and certified

	SAMUEL OBERSTEIN, M.D., Investigator & Assistant Medical Director DOWNLOAD CV Born in Cuba and fluent in Spanish, English and Yiddish, Dr. Oberstein attended Medical School at the Mount Sinai School of Medicine at CUNY, graduating with the MD degree with honors in 1971 and then completed his internship and residency in Obstetrics and Gynecology at the same institution. He is a Diplomate of the American Board of Obstetrics and Gynecology and Fellow of the American College of Surgeons. He has 12 years experience as a full time researcher in the area of Clinical Pharmacology and serves as Assistant Medical Director and one of the Investigators at Clinical Pharmacology of Miami.
	JESUS OLIVA CCRC, Project Manager & Senior Study Coordinator  DOWNLOAD CV Born in Cuba and fluent in Spanish and English, Jesus attended Rutgers University. He has 10 years experience in clinical study execution, most of it in Phase 1 Units. He is certified as a clinical research coordinator by the Association of Clinical Research Professionals.
	YAQUELIN RODRIGUEZ, CRC, FMG, Research Study Coordinator  DOWNLOAD CV Yaqueline was born and educated in Cuba and is fluent in both English and Spanish. She has over eight years experience as a Clinical Research Coordinator having worked in four different Phase 1 Facilities. Her background and experience combine to make her an outstanding coordinator who will effortlessly organize and execute even your most complex clinical research studies.
	HADAZA CATALA, Data Entry & Regulatory Affairs Manager  Fluent in English and Spanish, Hadaza has eight years experience in clinical research. She has attended numerous courses and seminars on Informed Consent Form preparation, certification and administration. She prepares all of our IRB submissions and oversees the informed consent process as well as being a very competent data entry manager.
	MARIA VICTORIA QUINONES,  Data Entry Manager and Quality Control Coordinator
	YOLAINA CRUZ, Pharmacokinetic Laboratory Manager
	YANET HERRERA, Assistant Study Coordinator
	YENY RAMOS, Assistant Study Coordinator
	DIANA FERNANDEZ, Receptionist and Screening Recruiter