Senior Manager, Statistical Programming – Clinical Trials

Regeneron Pharmaceuticals, Inc (USA); Kentucky; On-site; USD 129,000 - 210,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc (USA) seeks a Manager, Statistical Programming to lead programming deliverables for studies through regulatory approval, product launch, and annual reports. You will collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analyses and reporting.

The role requires a Master's 6+ years (or BS 7+ years) in a relevant field, proven leadership in clinical-study programming, and strong organizational skills within a regulated

Qualifications

• Master's degree with 6+ years (or BS 7+) of relevant work experience.
• Proven experience leading programming deliverables within a clinical study team.
• Experience providing input on hiring, feedback, and performance evaluation.
• Strong organizational and documentation skills within a regulated environment.

Responsibilities

• Lead programming deliverables from a single study through regulatory approval, launch, and annual reports.
• Oversee development and quality control of tables, listings, and graphs.
• Manage programming effort and track progress of deliverables.
• Serve as programming representative on multidisciplinary study teams.
• Collaborate with management on resource requirements for your area.
• Assist in hiring by reviewing resumes and screening candidates.

Skills

Program leadership

Cross-functional collaboration

Project tracking

Study team liaison

Resource planning

Hiring involvement

Performance feedback

Data governance

Communication

Analytical thinking

Specialization

Adaptability

Regulated documentation

Leadership

Education

Master's degree in a related field

Bachelor's degree in a related field

Tools

SAS Certification

Job description

Regeneron Pharmaceuticals, Inc (USA) seeks a Manager, Statistical Programming to lead programming deliverables for studies through regulatory approval, product launch, and annual reports. You will collaborate with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analyses and reporting.

The role requires a Master's 6+ years (or BS 7+ years) in a relevant field, proven leadership in clinical-study programming, and strong organizational skills within a regulated