h3bSenior Pharmacovigilance Scientist (f/m/d) - Post-marketing products /b /h3h3Responsibilities: /h3ulliLead the safety review process and evaluation of safety data throughout the product lifecycle using a combination of quantitative and qualitative approaches, in partnership with the Global Safety Lead (GSL) /liliPerform end to end signal detection and analysis activities on safety data sets from various sources, and present summaries of the data in a meaningful way /liliReview publications from the scientific and medical literature for important safety information for further use in various analyses or aggregate safety reports (ASRs) /liliProvide strategic input and/or contributions to various ASRs (Periodic Safety Update Reports, Development Safety Update Reports, PADERs, Risk Management Plans etc.) /liliOrganize and provide key insight to internal cross functional Safety Management Teams (SMTss) /liliSupport product development teams (such as the Study Execution Team and the Clinical Development Teams) with PV related expertise relating to clinical data /liliDevelop response strategy and perform required analyses for any safety-related questions from internal sources and/or external regulatory requests /liliMentor more junior members of the PVS community, including assisting with on-boarding and providing advice on day-to-day tasks /liliOther Activities as required, including but not limited to: case adjudication, review of key clinical documents (IBs, CSRs, etc), support in SOP updates, subject matter expert support for dedicated PVS activities, etc /li /ulh3Qualifications: /h3ulliBachelor’s or equivalent degree (depending on national educational system) required in the pharmaceutical, nursing or biological, or sciences (Degree in Medicine and Pharmacy is preferred) /liliAt least 3 years’ experience as a Pharmacovigilance scientist or equivalent position in a closely related discipline /liliUnderstanding of pharmacovigilance and global clinical safety methodology and regulations, guidelines, and standards. /liliAbility to provide solutions for issues/challenges that may arise during the course of a project /liliKnowledge and experience of safety monitoring and signal detection preferred. /liliUnderstanding of ICH GCP and drug development preferred /liliComputer proficiency in basic database entry and graphics presentations (e.g.,Microsoft Excel or equivalent). /liliExcellent written and verbal communication skills in English, with the ability to evaluate, interpret and synthesize scientific data. /liliSelf-motivated, able to prioritize and plan effectively /liliAbility to work independently and as a team player, working in a cross functional environment /li /ulpDifferent qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable. /p #J-18808-Ljbffr
Senior Pharmacovigilance Scientist (f/m/d) - Post-marketing products Research Development & Sciences Pharmacovigilance Operations CSL Behring Glattbrugg, Switzerland R-293519 Posted on October 27, 2026 Arbeitgeber: CSL
Unser Unternehmen bietet eine dynamische und unterstützende Arbeitsumgebung, die sich auf die Förderung von Innovation und Exzellenz in der analytischen Wissenschaft konzentriert. Mit einem starken Fokus auf Mitarbeiterentwicklung und kontinuierlichem Lernen bieten wir zahlreiche Möglichkeiten zur beruflichen Weiterentwicklung, während wir gleichzeitig ein positives und kollaboratives Arbeitsklima pflegen. Unsere Lage in einer hochmodernen Einrichtung ermöglicht es Ihnen, an vorderster Front der pharmazeutischen Forschung zu arbeiten und einen bedeutenden Beitrag zur Verbesserung der Gesundheitsversorgung zu leisten.
