Elizabeth Kurian
Diversity, equality, and inclusion advocate, Pharmacovigilance and patient safety specialist, Collaborative leadership adept
- Role
- Director, Serm at GSK
- Location
- Chicago, IL, US
- LinkedIn followers
- 500 followers
About Elizabeth Kurian
Patient safety specialist with a strong foundation in clinical, regulatory, and business management. Passionate about utilizing my expertise to provide health care professionals with clinical data to drive positive outcomes. Pharmacist with over 10 years of patient care specializing in immunology, virology, and general medicine, combined with over eight years of experience in pharmacovigilance and patient safety in the biopharmaceutical research & development industry. Well versed in the end-to-end drug development and commercialization lifecycle, alongside a deep understanding of disease terminology and drug development regulatory requirements. Strong business and medical acumen, combined with high emotional intelligence, lends to an ability to clearly communicate medical concepts to a wide variety of audiences. Extensive experience performing medical document reviews and analyses on clinical and post-market safety data. Tech-forward business leader known for championing technology innovations to streamline operations and increase workflow efficiencies. Languages: English, Spanish, and Malayalam
Experience
Director, Serm
Oct 2021 — Present
As a Director in SERM, I am involved with the benefit risk profile of our products for the entire lifecycle. This offers an impactful contribution of pharmacovigilance and risk management from a variety of perspectives to numerous product teams-Drives pharmacovigilance and risk management planning in the clinical matrix and leads production of global Benefit-Risk Management Plans for designated products-Delivers the clinical safety input into clinical development planning activities-Reviews and provides technical approval for investigator brochures, protocols, Informed consents, final study reports and external data monitoring committee charters-May lead or participate in discussion at Global Safety Board / Consumer Products Safety Board for safety related findings in clinical development-Presents safety information at clinical investigator and commercial meetings-Ensures prompt notification to SERM Head of reviewed protocols that are identified as potential PASS-Overseeing surveillance and regulatory activities for assigned products and therapeutic areas
Education
University of the Sciences in Philadelphia
Doctor of Pharmacy (PharmD)
1999 — 2005
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