Senior Manager, Statistical Programming – Lead & Mentor

BioSpace; Cambridge (MA); On-site; USD 151,000 - 246,000; Full time

Job summary

Regeneron is seeking a Senior Manager, Statistical Programming to lead analytical programming on our clinical portfolio. You will oversee deliverables from single studies through regulatory submission, product launch, and annual reports, collaborating with study teams, CROs, and colleagues to standardize programming approaches.

The role emphasizes data modeling, programming standards, mentoring, and ensuring timely, high-quality support across regulatory milestones.

Qualifications

• Master's degree with 8-10 years of relevant experience.
• Proven experience leading programming deliverables within a clinical or therapeutic area.
• Strong mentoring and team collaboration skills.
• Experience developing and applying programming standards and data models.

Responsibilities

• Coordinate and oversee analysis programming within your therapeutic area, tracking progress and completion of deliverables.
• Manage and coordinate programming and quality control of analysis datasets and outputs in support of regulatory submissions.
• Mentor others on the use of standardization tools and therapeutic area standard analysis approaches.
• Serve as the programming representative on a multidisciplinary study team, ensuring timely, quality support through regulatory approval and launch.
• Develop data models, programming standards, and code, and train end users on project standards.
• Mentor junior staff, fostering a collaborative environment and modeling strong team behavior.
• Contribute to programming development and quality control using established tools and methodologies.
• Advise team members on procedures for data, records, and information retention.

Skills

Programming leadership

Mentoring

Data modeling

Standards development

Regulatory submissions

Education

Master's degree

Tools

SAS

Job description

Regeneron is seeking a Senior Manager, Statistical Programming to lead analytical programming on our clinical portfolio. You will oversee deliverables from single studies through regulatory submission, product launch, and annual reports, collaborating with study teams, CROs, and colleagues to standardize programming approaches.

The role emphasizes data modeling, programming standards, mentoring, and ensuring timely, high-quality support across regulatory milestones.