Manager, Case Processing

Johnson & Johnson MedTech

Allschwil, Basel-Country, Switzerland
On-site
Global medical safety operations
Investigational clinical trial icsrs
Serious and unexpected suspected adverse reaction reporting
Johnson & Johnson MedTech is seeking a Manager, Case Processing in Allschwil, Switzerland, to lead a team responsible for processing individual case safety reports (ICSRs) related to clinical trials. The ideal candidate will have extensive experience in pharmacovigilance and drug safety, along with strong leadership and people management skills

Job Summary

  • Directly lead the daily operational activities of a Global Case Processing team within Global Medical Safety Operations, ensuring effective workload management and adherence to ICSR quality and timeline standards.
  • Manage and support team members in day-to-day case processing activities through coaching, guidance, performance management, and ongoing staff development.
  • Ensure the quality, accuracy, and regulatory compliance of team-processed ICSRs, with particular focus on SUSAR reporting requirements, including completeness of case narratives, coding activities, AOSE, and related documentation.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Manager, Case Processing in Allschwil, Switzerland, to lead a team responsible for processing individual case safety reports (ICSRs) related to clinical trials. The ideal candidate will have extensive experience in pharmacovigilance and drug safety, along with strong leadership and people management skills.

Skills & Requirements

Must-have

  • Global Medical Safety Operations
  • Investigational Clinical Trial ICSRs
  • Serious and Unexpected Suspected Adverse Reaction reporting
  • Quality and timeline standards
  • Pharmacovigilance safety systems

Nice-to-have

  • Credo-based values
  • Ethical decision-making
  • Process improvements
  • Motivate teams
  • Manage change

Key Requirements

  • Bachelor’s degree in a health-related or scientific discipline
  • Minimum of 5 years of pharmaceutical industry or clinical experience
  • Demonstrated knowledge of global safety reporting regulations
  • Demonstrated people-management capability
  • Proficiency with standard office applications

Work Rights

Not specified

Tailored Resume

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