Gustavo Gomez, Ccra
About Gustavo Gomez, Ccra
Gustavo Gomez is a Clinical Research Associate II (CCRA) at Supernus Pharmaceuticals, Inc., where he has worked since 2015. He is responsible for training co-workers on Phase I-III studies and overseeing Contract Research Organizations.
Work at Supernus Pharmaceuticals
Gustavo Gomez has been employed at Supernus Pharmaceuticals, Inc. as a Clinical Research Associate II CCRA since 2015. In this role, he is responsible for training co-workers on studies ranging from Phase I to Phase III. He assists in overseeing Contract Research Organizations (CROs) and other study vendors, which includes co-monitoring external CRO monitors. His position requires active participation in the identification and recruitment of investigators and the development of subject recruitment strategies and materials. He serves as the primary point of contact for study site personnel, addressing questions and resolving study-related issues.
Education and Expertise
Gustavo Gomez earned his Bachelor's degree from Great Basin College, completing his studies from 2013 to 2017. He has furthered his professional development by completing courses such as 'Clinical Project Management: Fundamentals of Project Management' and both 'Mon Clinical Drug Studies: Beginner Course' and 'Mon Clinical Drug Studies: Advanced Course.' His expertise is recognized through his certification as a Clinical Research Associate, which he obtained in February 2020 from the Association of Clinical Research Professionals (ACRP).
Background
Before joining Supernus Pharmaceuticals, Gustavo Gomez worked at Sigma-Tau Pharmaceuticals, Inc. as a Clinical Research Specialist from 2014 to 2015. His career in the pharmaceutical industry began at Otsuka Pharmaceutical Companies (U.S.), where he served as an Administrative Service Assistant from 2008 to 2013. His experience spans various roles that have contributed to his knowledge and skills in clinical research and project management.
Achievements
Gustavo Gomez has made significant contributions to the field of clinical research through his roles in various pharmaceutical companies. His responsibilities include training co-workers, overseeing CROs, and developing recruitment strategies for clinical studies. His certification as a Clinical Research Associate and completion of specialized courses further demonstrate his commitment to professional growth and excellence in clinical research practices.