IQVIA RDS GmbH
Regulatory Affairs Specialist(m/w/x)
Full-timeOn-siteExperienced
Frankfurt am Main
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SASanofi-Aventis Deutschland GmbH
PV Literature Surveillance Expert(m/w/x)
Frankfurt am Main
Full-timeOn-siteExperienced
AI/ML
Nejo AI Summary
Overseeing literature screening platforms and vendor activities for cardiovascular drug safety. International pharmacovigilance background and literature assessment experience essential. Cutting-edge technology platforms, international team collaboration.
Requirements
- Pharm.D., bachelor's in health science, or related
- Background in international pharmacovigilance or clinical development
- Experience surveilling and assessing literature for safety
- Knowledge of safety reports and risk management
- Computer literacy with Windows-based programs
- Familiarity with literature screening platforms
- Knowledge of worldwide safety reporting regulations
- Ability to work in global environments
- Strong teamwork and stakeholder management capabilities
- Effective organization and multitasking skills
- Strategic thinking and process improvement mindset
- Excellent English communication skills
Tasks
- Support the Global Lead in managing surveillance resources
- Manage vendor activities for literature screening and quality
- Oversee technology teams managing the screening platform
- Develop search strategies with Global Safety Operations
- Coordinate literature needs for safety reports and signal detection
- Serve as subject matter expert during audits and inspections
- Execute routine and ad-hoc literature surveillance activities
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- Windows
- Literature screening platforms
Benefits
Modern Equipment
- Cutting-edge technology platforms
Other Benefits
- Innovative pharmacovigilance approaches
Informal Culture
- Collaborative international teams
Learning & Development
- Continuous learning opportunities
- Professional development
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Sanofi-Aventis Deutschland GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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SASanofi-Aventis Deutschland GmbH
PV Literature Surveillance Expert(m/w/x)
Frankfurt am Main
Full-timeOn-siteExperienced
AI/ML
Nejo AI Summary
Overseeing literature screening platforms and vendor activities for cardiovascular drug safety. International pharmacovigilance background and literature assessment experience essential. Cutting-edge technology platforms, international team collaboration.
Requirements
- Pharm.D., bachelor's in health science, or related
- Background in international pharmacovigilance or clinical development
- Experience surveilling and assessing literature for safety
- Knowledge of safety reports and risk management
- Computer literacy with Windows-based programs
- Familiarity with literature screening platforms
- Knowledge of worldwide safety reporting regulations
- Ability to work in global environments
- Strong teamwork and stakeholder management capabilities
- Effective organization and multitasking skills
- Strategic thinking and process improvement mindset
- Excellent English communication skills
Tasks
- Support the Global Lead in managing surveillance resources
- Manage vendor activities for literature screening and quality
- Oversee technology teams managing the screening platform
- Develop search strategies with Global Safety Operations
- Coordinate literature needs for safety reports and signal detection
- Serve as subject matter expert during audits and inspections
- Execute routine and ad-hoc literature surveillance activities
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- Windows
- Literature screening platforms
Benefits
Modern Equipment
- Cutting-edge technology platforms
Other Benefits
- Innovative pharmacovigilance approaches
Informal Culture
- Collaborative international teams
Learning & Development
- Continuous learning opportunities
- Professional development
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Sanofi-Aventis Deutschland GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Sanofi-Aventis Deutschland GmbH
Industry
Pharmaceuticals
Description
Das Unternehmen bietet Arzneimittel zur Prävention von Herz-Kreislauf-Erkrankungen an und setzt sich für die Verbesserung der Lebensqualität ein.
Not a perfect match?
- IQVIA RDS GmbH
Regulatory Affairs Specialist(m/w/x)
Full-timeOn-siteExperiencedFrankfurt am Main - 100055 Fresenius Kabi Deutschland GmbH
Program Manager - Digital & AI Projects(m/w/x)
Full-timeOn-siteExperiencedBad Homburg vor der Höhe - Roche Pharma AG
Global Medical Collaboration Leader - Cardiovascular(m/w/x)
Full-timeOn-siteExperiencedFrankfurt am Main - IQVIA
Principal Medical Writer – Clinical Pharmacology(m/w/x)
Full-timeOn-siteExperiencedFrankfurt am Main - 100055 Fresenius Kabi Deutschland GmbH
Process Architect Quality Management / Complaint Management(m/w/x)
Full-timeOn-siteExperiencedBad Homburg vor der Höhe