Manager, Case Processing

Johnson & Johnson

Horsham, Pennsylvania, United States of America
$117,000.00 - $201,250.00 py
Hybrid
Drug safety associates management
Investigational ct icsr processing
Susar reporting requirements
Johnson & Johnson is seeking a Manager, Case Processing to oversee the operational activities of a team focused on processing safety reports for clinical trials. The ideal candidate will have a strong background in pharmacovigilance, team leadership experience, and a commitment to regulatory compliance

Job Summary

  • Directly leading 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.
  • Managing and supporting team members in day-to-day case processing activities through coaching, guidance, performance management, and ongoing staff development.
  • Ensuring 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 is seeking a Manager, Case Processing to oversee the operational activities of a team focused on processing safety reports for clinical trials. The ideal candidate will have a strong background in pharmacovigilance, team leadership experience, and a commitment to regulatory compliance.

Salary

$117,000.00 - $201,250.00

Skills & Requirements

Must-have

  • Drug Safety Associates management
  • Investigational CT ICSR processing
  • SUSAR reporting requirements
  • Quality and timeline adherence
  • Global safety reporting regulations

Nice-to-have

  • Cross-functional collaboration
  • Developing others
  • Inclusive leadership
  • Ethical decision-making

Key Requirements

  • Bachelor’s degree in health-related or scientific discipline
  • Active professional licensure/certification for nurses or pharmacists
  • Minimum of 5 years of pharmaceutical industry or clinical experience
  • Demonstrated people-management capability
  • Proficiency with pharmacovigilance safety systems

Work Rights

Not specified

Tailored Resume

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