CRA, Class III Medical Device (Coronary Stents) @ Medtronic
Clinical Research Coordinator then CRA Monitor (Rheumatology and Oncology) @ EBR Research Institute
New Product Dev't Professional (Diabetes, Infectious Diseases, Vaccines) @ GSK
Jolly Carpena's Education
UC BERKELEY
Project Management in Life Sciences (Project Management)
2014 - 2015
VIP Nursing School, San Leandro, California
Associate in Nursing
2009 - 2010
University of California - Berkeley
Clinical Research Conduct and Management
2007 - 2008
Iloilo Doctors' College - Philippines
Bachelor of Science in Nursing (BSN)
2001 - 2003
University of St. La Salle
Master of Business Administration (MBA)
1998 - 2001
University of St La Salle
Bachelor of Arts in Mass Communications
1983 - 1988
Jolly Carpena's Skills
Strategic Planning
Project Management
Clinical Development
CRO
Site Management. Currently Manages 50 Sites All Across the Us
Clinical Monitoring
Clinical Trial Management System Ctms
Socra
FDA
Medical Devices
Jolly Carpena's Summary
Jolly Carpena, based in California, United States, is currently a GCP compliance expert and Consultant on Inspection Readiness of the Trial Master File at Biotech, Pharma, & Medical Device, bringing experience from previous roles at Nektar Therapeutics, BioMarin Pharmaceutical Inc., Abbott and Direct Flow MedicalĀ®, Inc.. Jolly Carpena holds a 2014 - 2015 Project Management in Life Sciences in Project Management @ UC BERKELEY. With a robust skill set that includes Strategic Planning, Project Management, Clinical Development, CRO, Site Management. Currently Manages 50 Sites All Across the Us and more, Jolly Carpena contributes valuable insights to the industry. Jolly Carpena has 2 emails and 1 mobile phone number on RocketReach.