Associate Medical Safety Director- Sponsor Dedicated
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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 periodic safety reports, risk management plans, regulatory submissions, labeling, protocols, investigator brochures, and case report forms.
Support safety
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São Domingos De Rana, Portuguese Republic, Portugal Iqvia Tempo integralConduct 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 periodic safety...
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Paço De Arcos, Portuguese Republic, Portugal Iqvia Tempo integralIQVIA 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,...
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São Domingos De Rana, Portuguese Republic, Portugal Iqvia Tempo integralIQVIA 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,...
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Paço De Arcos, Portuguese Republic, Portugal Iqvia Tempo integralIQVIA 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,...
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São Domingos De Rana, Portuguese Republic, Portugal Iqvia Tempo integralIQVIA 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,...
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Senior Site Contract Associate
Há 2 dias
são joão de lourosa, viseu, Portugal IQVIA Biotech Tempo integralSenior Site Contracts Associate IQVIA Biotech France, Spain, Portugal & Greece - HomebasedIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that...