Global Patient Safety Leader: Signals & Risk Analytics

Regeneron Pharmaceuticals, Inc (USA); Kentucky; On-site; USD 115,000 - 187,000; Full time

Benefits offered by this job

Annual bonus or incentive plans

Equity awards

Pension or retirement benefits

401(k) company match

Health and wellness programs

Fitness centers

Insurance benefits (medical, dental,)

Paid time off

Family support benefits

Job summary

Regeneron Pharmaceuticals, Inc (USA) is seeking a Manager for Global Patient Safety Sciences in a 4-day on-site role based in Sleepy Hollow, NY, Warren, NJ, or Cambridge, MA with ~25% travel. You will lead safety strategies for molecules in development and post-marketing, including data aggregation and safety interpretation.

You will drive signal detection/evaluation, prepare safety documents, and present at SMT meetings. Strong data analysis and cross-functional collaboration are essential.

Qualifications

• Minimum Master degree, PharmD, or PhD.
• Safety or relevant clinical experience in pharma/biotech required, typically 5+ years.
• Experience with pharmacovigilance and safety surveillance appreciated.

Responsibilities

• Complete signal detection activities per safety surveillance plan.
• Perform signal evaluation and author safety evaluation reports.
• Prepare and review DSUR, PSUR, and RMP documents.
• Deliver presentations at SMT meetings and participate in study teams.
• Engage in risk management activities for assigned compounds.
• Represent GPS on cross-functional teams and committees.
• Utilize Excel and pivot tables for safety data analysis.
• Contribute to process improvements and SOP development.

Skills

Signal detection

Signal evaluation

Safety data analysis

Data visualization

Presentations

Cross-functional teamwork

Communication

Education

Master's degree

PharmD

PhD

Tools

Excel

Pivot tables

Job description

Regeneron Pharmaceuticals, Inc (USA) is seeking a Manager for Global Patient Safety Sciences in a 4-day on-site role based in Sleepy Hollow, NY, Warren, NJ, or Cambridge, MA with ~25% travel. You will lead safety strategies for molecules in development and post-marketing, including data aggregation and safety interpretation.

You will drive signal detection/evaluation, prepare safety documents, and present at SMT meetings. Strong data analysis and cross-functional collaboration are essential.