Portia C. is a seasoned Pharmacovigilance Specialist with extensive experience in case management and regulatory compliance within the pharmaceutical industry. Currently at Seqirus since May 2021, Portia C. oversees pharmacovigilance activities for in-licensed products, utilizing expertise in clinical trial SAE management and regulatory submissions. Prior roles include positions at MSD in the UK, The Janssen Pharmaceutical Companies of Johnson & Johnson, GSK, and AbbVie, where Portia C. demonstrated proficiency in adverse event reporting, inspection readiness, and quality assurance. Portia C. holds a Master of Pharmacy degree from The University of Manchester.
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