Serious and unexpected suspected adverse reaction (susar) reporting
Global medical safety operations (gmso) functions
**
Johnson & Johnson is seeking a Manager of Case Processing in High Wycombe, UK, to oversee a team responsible for processing clinical trial safety reports. The ideal candidate should have a background in pharmacovigilance, strong leadership skills, and a commitment to compliance and quality standards.
**
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.
Responsibilities include directly leading daily operational activities, managing and supporting team members, ensuring quality and regulatory compliance of processed ICSRs, and performing people-management responsibilities.
Matching Summary
Match Score: 75
**
Johnson & Johnson is seeking a Manager of Case Processing in High Wycombe, UK, to oversee a team responsible for processing clinical trial safety reports. The ideal candidate should have a background in pharmacovigilance, strong leadership skills, and a commitment to compliance and quality standards.
**
Skills & Requirements
Must-have
Drug Safety Associates (DSAs)
Serious and Unexpected Suspected Adverse Reaction (SUSAR) reporting
Global Medical Safety Operations (GMSO) functions
Clinical trial case processing
Pharmacovigilance regulations
Nice-to-have
Credo-based values
Ethical decision-making
Inclusive work environment
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