Temple University School of Pharmacy
MASTER OF SCIENCE IN GLOBAL CLINICAL AND PHARMACOVIGILANCE REGULATIONS (GCPR)
Philadelphia, USA
MSc
DURATION
LANGUAGES
English
PACE
APPLICATION DEADLINE
EARLIEST START DATE
Sep 2026
STUDY FORMAT
Key Summary
About: The Master of Science in Global Clinical and Pharmacovigilance Regulations (GCPR) focuses on the regulatory frameworks governing clinical trials and the monitoring of adverse drug reactions. This program prepares students to navigate the complexities of drug development and safety, ensuring compliance with international standards.
Career Outcomes: Graduates can pursue careers in pharmaceutical companies, regulatory agencies, and clinical research organizations. Potential job roles include regulatory affairs specialist, clinical research coordinator, and pharmacovigilance officer.
The MS in Global Clinical and Pharmacovigilance Regulations focuses on both disciplines of clinical trials and pharmacovigilance, enabling PharmD and MD graduates to pursue positions in the U.S. and global clinical trial projects, research administrators, and safety directors in the global marketplace. The curriculum provides the skills needed to manage and oversee clinical trials, supervise record-keeping, review clinical trial or post-marketing safety data, and interpret results.
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