Temp Mgr Global Patient Safety Sciences

What you’d do

Perform signal detection and evaluation, author safety evaluation reports, and manage safety documents such as DSUR, PSUR and RMP. Present at Signal Management Team meetings and represent Global Patient Safety Sciences on cross-functional teams. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• 5+ years risk management or clinical experience in pharma/biotech or health authority
• Previous safety or relevant clinical experience in pharmaceutical industry
• Data manipulation and visualization (Excel, PIVOT tables)
• Author safety evaluation reports and safety documents
• Full time