Senior Statistical Programming Lead

BioSpace; Cambridge (MA); On-site; USD 129,000 - 210,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

Pension benefits

401k match

Health benefits

Wellness programs

Fitness centers

Paid time off

Family support

Job summary

Regeneron is seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study from initial analysis through regulatory approval, product launch, and annual reports. Location options include Warren, NJ or Cambridge, MA with an onsite work model.

You will lead the development and QC of tables, listings, and graphs, manage programming resources, and collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analyses and

Qualifications

• Master's degree required with 8–10 years experience (or a Master's in Statistics/CS/Math/Engineering/Life Science with 5+ years of programming and some project/people management).
• Proven experience leading programming deliverables within a clinical study team.
• Experience providing input on hiring, feedback, and performance evaluation.
• Strong organizational and documentation skills in a regulated environment.
• Nice to have: SAS Certification.

Responsibilities

• Lead programming deliverables from a single study through regulatory approval and launch.
• Coordinate development and QC of tables, listings, and graphs for analysis requirements.
• Manage programming effort and track progress of deliverables, including ad hoc requests.
• Serve as programming representative on a multidisciplinary study team.
• Collaborate with management to determine resource needs.

Skills

Clinical study programming leadership

Program deliverables management

Hiring & performance feedback

Documentation in regulated env

SAS Certification (nice to have)

Education

Master's degree

Tools

SAS

Job description

Regeneron is seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study from initial analysis through regulatory approval, product launch, and annual reports. Location options include Warren, NJ or Cambridge, MA with an onsite work model.

You will lead the development and QC of tables, listings, and graphs, manage programming resources, and collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analyses and