Lori Medeiros

Senior Director, Pharmacovigilance @Worldwide Clinical Trials

Wilmington, NC, US
EMAILS
l••••••••@worldwide.com
MOBILE NUMBERS
+19•••••••50

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WORK HISTORY

Mar 2025 — Present

Senior Director, Pharmacovigilance @Worldwide Clinical Trials

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EDUCATION

2001 — 2003

University of North Carolina Wilmington

Bachelor of Science, Nursing

1996 — 2000

University of North Carolina Wilmington

Bachelor of Science, Biology

SKILLS

PharmacovigilanceCROPharmaceutical IndustrySopDrug SafetyGcpIch-GcpEdcOncologyCtmsClinical ResearchRegulatory SubmissionsClinical Trials

ABOUT LORI MEDEIROS

I am an Associate Director of Pharmacovigilance with 14 years of experience working for several large global CROs within drug safety/pharmacovigilance. Direct experience with processing serious and non-serious adverse events for clinical trials (phases I-IV) including end point adjudication; processing for post marketing serious and non-serious adverse events; project set-up for global clinical trials/programs; generate, track, and distribute regulatory reports and cross reports; line management; management of project and department budgets; and development of SOP/WIs.

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