Global Medical Safety Director: Lead Strategy

IQVIA in Portugal is seeking a Global Safety Physician to lead medical safety activities across clinical development and post‑marketing programs. The role encompasses oversight of safety data reviews, regulatory submissions, risk management and cross‑functional collaboration. As a project leader, you will mentor safety teams, ensure timely delivery,...

IQVIA is seeking a Global Safety Physician to lead medical safety activities across clinical development and post-marketing programs. You will oversee safety data reviews, regulatory safety reporting, and risk management strategies while guiding a global team of physicians and safety professionals. Engage with clients and internal stakeholders to ensure...

Responsibilities Conduct medical review of clinical trial and post-marketing safety data, including adverse events (AEs), adverse drug reactions (ADRs), coding, causality, expectedness, seriousness assessments, and benefit-risk evaluations. Provide medical oversight and review of safety documentation, including narratives, aggregate reports, annual and...

Job Overview The Senior Medical Director provides strategic medical and scientific subject matter experience and expertise to IQVIA in the specialty/subspecialty or therapeutic area for which they have first hand knowledge informed by training, experience and expertise. They gain greater independence over time for various activities that include but are not...

Job Overview The Senior Medical Director provides strategic medical and scientific subject matter experience and expertise to IQVIA in the specialty/subspecialty or therapeutic area for which they have first hand knowledge informed by training, experience and expertise. They gain greater independence over time for various activities that include but are not...

IQVIA’s Lifecycle Safety Medical team in Portugal seeks an Associate Medical Safety Director to lead medical safety activities, oversee signal detection, benefit-risk evaluation, and regulatory reporting for assigned portfolios. You will provide pharmacovigilance expertise, mentor teams, and ensure compliant safety oversight across study protocols,...

IQVIA’s Lifecycle Safety Medical team is seeking an Associate Medical Safety Director to oversee safety reviews, signal detection, risk management, and regulatory safety documentation for portfolio products. You will lead medical reviews, contribute to regulatory safety reports, and provide expert safety support across study and post-marketing activities,...

IQVIA is seeking an Associate Medical Safety Director to join its Lifecycle Safety Medical team in Portugal. You will oversee safety data reviews, lead signal detection, and contribute to regulatory safety reports. The role requires a medical degree and about three years of clinical practice plus industry experience, strong regulatory knowledge, and the...

Responsibilities Conduct medical review of clinical trial and post-marketing safety data, including adverse events (AEs), adverse drug reactions (ADRs), coding, causality, expectedness, seriousness assessments, and benefit-risk evaluations. Provide medical oversight and review of safety documentation, including narratives, aggregate reports, annual and...