Manager, Case Processing

Johnson & Johnson

Horsham, Pennsylvania, United States of America
Base: $117,000.00 - $201,250.00; bonus/equity: not...
Hybrid
Drug safety associates (dsas)
Investigational ct icsrs
Susar reporting requirements
The Manager, Case Processing directs and oversees the operational and people management activities of a team of Drug Safety Associates (DSAs) responsible for processing investigational Clinical Trial (CT) Individual Case Safety Reports (ICSRs)

Job Summary

  • The Manager, Case Processing directs and oversees the operational and people management activities of a team of Drug Safety Associates (DSAs) responsible for processing investigational Clinical Trial (CT) Individual Case Safety Reports (ICSRs).
  • This role partners closely with Global Medical Safety Operations (GMSO) functions and Clinical Development organizations to enable compliant, timely, and efficient end-to-end management of investigational CT ICSRs.
  • The position requires a Bachelor’s degree in a health-related or scientific discipline with a minimum of 5 years of pharmaceutical industry or clinical experience with a focus on pharmacovigilance and drug safety.

Matching Summary

The Manager, Case Processing directs and oversees the operational and people management activities of a team of Drug Safety Associates (DSAs) responsible for processing investigational Clinical Trial (CT) Individual Case Safety Reports (ICSRs).

Salary

Base: $117,000.00 - $201,250.00; Bonus/Equity: Not specified; Benefits: Vacation, Sick time, Holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off

Skills & Requirements

Must-have

  • Drug Safety Associates (DSAs)
  • Investigational CT ICSRs
  • SUSAR reporting requirements
  • Global Medical Safety Operations
  • Pharmacovigilance regulations

Nice-to-have

  • Credo-based values
  • Ethical decision-making
  • Inclusive work environment

Key Requirements

  • Bachelor’s degree in health-related or scientific discipline
  • Minimum 5 years of pharmacovigilance/drug safety experience
  • Demonstrated people-management capability
  • Knowledge of global safety reporting regulations

Work Rights

Not specified

Tailored Resume

Cover Letter