The AI Job Search Engine
Medical Director Safety(m/w/x)
Description
You will lead safety strategies for clinical research, ensuring regulatory compliance while managing risk assessments and signal detection to protect patients across the company's diverse nutritional portfolio.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical degree, MD/PhD, or preferred specialization
- •Swiss medical practice license as plus
- •Experience in clinical research and safety
- •Leadership in complex clinical trial safety
- •Expertise in clinical safety assessments
- •Strong strategic acumen and cross-functional collaboration
- •Ability to analyze complex scientific information
- •Effective external engagement capabilities
- •Balance of urgency, quality, and compliance
Education
Tasks
- •Provide expert safety leadership for clinical development programs
- •Ensure compliance with pharmaceutical and medical nutrition regulatory frameworks
- •Build safety assessments and management plans for trial designs
- •Conduct signal detection, monitoring, and evaluation of safety data
- •Manage and report safety information including annual safety reports
- •Lead safety input for DSMB charters and aggregate safety reports
- •Contribute to risk management plans and signal review forums
- •Coordinate internal trial safety boards and committees
- •Drive safety strategies in collaboration with cross-functional teams
- •Manage external providers responsible for case processing
- •Engage with investigators and key opinion leaders to shape strategies
- •Respond to safety inquiries and health authority requests
- •Support end-to-end pharmacovigilance for nutrition therapeutics
- •Align safety activities with internal risk management governance
Languages
English – Business Fluent
Benefits
Flexible Working
- •Flexible working arrangements
Career Advancement
- •Career development opportunities
Informal Culture
- •Respectful, diverse, and inclusive culture
Startup Environment
- •Dynamic international environment
- MedtronicFull-timeOn-siteExperiencedLausanne
- SHQ Medtronic Int. Trading Sàrl
Regulatory Affairs Specialist(m/w/x)
Full-timeOn-siteExperiencedLausanne - Société des Produits Nestlé S.A.
Health Solutions Specialist Physiology & Microbiome(m/w/x)
Full-timeOn-siteExperiencedLausanne - Société des Produits Nestlé S.A.
Associate Specialist Statistics(m/w/x)
Full-timeOn-siteExperiencedLausanne - SICPA SA
Managing Director - Identity & Compliance Vertical(m/w/x)
Full-timeOn-siteSeniorPrilly
Medical Director Safety(m/w/x)
The AI Job Search Engine
Description
You will lead safety strategies for clinical research, ensuring regulatory compliance while managing risk assessments and signal detection to protect patients across the company's diverse nutritional portfolio.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Medical degree, MD/PhD, or preferred specialization
- •Swiss medical practice license as plus
- •Experience in clinical research and safety
- •Leadership in complex clinical trial safety
- •Expertise in clinical safety assessments
- •Strong strategic acumen and cross-functional collaboration
- •Ability to analyze complex scientific information
- •Effective external engagement capabilities
- •Balance of urgency, quality, and compliance
Education
Tasks
- •Provide expert safety leadership for clinical development programs
- •Ensure compliance with pharmaceutical and medical nutrition regulatory frameworks
- •Build safety assessments and management plans for trial designs
- •Conduct signal detection, monitoring, and evaluation of safety data
- •Manage and report safety information including annual safety reports
- •Lead safety input for DSMB charters and aggregate safety reports
- •Contribute to risk management plans and signal review forums
- •Coordinate internal trial safety boards and committees
- •Drive safety strategies in collaboration with cross-functional teams
- •Manage external providers responsible for case processing
- •Engage with investigators and key opinion leaders to shape strategies
- •Respond to safety inquiries and health authority requests
- •Support end-to-end pharmacovigilance for nutrition therapeutics
- •Align safety activities with internal risk management governance
Languages
English – Business Fluent
Benefits
Flexible Working
- •Flexible working arrangements
Career Advancement
- •Career development opportunities
Informal Culture
- •Respectful, diverse, and inclusive culture
Startup Environment
- •Dynamic international environment
About the Company
Société des Produits Nestlé S.A.
Industry
Food
Description
The company develops new products, processes, and packaging concepts for a broad range of Nutrition, Dairy, Health Science, and Coffee products.
- Medtronic
Regulatory Affairs Specialist(m/w/x)
Full-timeOn-siteExperiencedLausanne - SHQ Medtronic Int. Trading Sàrl
Regulatory Affairs Specialist(m/w/x)
Full-timeOn-siteExperiencedLausanne - Société des Produits Nestlé S.A.
Health Solutions Specialist Physiology & Microbiome(m/w/x)
Full-timeOn-siteExperiencedLausanne - Société des Produits Nestlé S.A.
Associate Specialist Statistics(m/w/x)
Full-timeOn-siteExperiencedLausanne - SICPA SA
Managing Director - Identity & Compliance Vertical(m/w/x)
Full-timeOn-siteSeniorPrilly