Sr. Analyst, Statistical Programming
Biogen
August 21, 2026
Remote friendly (Triangle, NC)
United States
Clinical Research and Development
Hybrid role (weekly in-person workdays). Location: Durham, NC or Cambridge, MA.
About This Role
The Senior Analyst, Statistical Programming leads and oversees statistical programming activities (internally and via vendors) to apply data standards; produce analysis datasets and specifications (CDISC ADaM); create tables, listings, figures, electronic submission components, and ad hoc analyses. Partners with Biostatistics to deliver submission-ready outputs; provides input to the Portfolio Lead (PL) on study timelines, milestones, issue escalation, and resource needs. Leads study teams of statistical programmers, provides vendor communication/quality oversight, and represents Statistical Programming as a functional lead. Helps implement the Data Strategy and develops standard programming practices across studies.
What You’ll Do
- Lead, coordinate, and manage statistical programming deliverables (creation, review, completion, delivery).
- Author CDISC ADaM analysis dataset specifications; define/document endpoint algorithms.
- Manage end-to-end programming from CRF data to electronic submission; ensure compliance with submission standards.
- Serve as Statistical Programming Lead to achieve study milestones.
- Verify consistency and proper use of data, analysis, and submission standards.
- Inform team members on programming requirements, deliverable status, and resourcing.
Who You Are
Senior Analyst with strong statistical programming skills, attention to detail, and ability to manage competing priorities.
Required Skills
- Bachelor’s degree.
- 5+ years relevant data management/analysis experience.
- 5+ years SAS Base; 5+ years SAS STAT/GRAPH/MACRO.
- 5+ years relevant industry experience; 5+ years clinical trial experience; 3+ years clinical database experience.
- CDISC and/or submissions experience.
- Knowledge of drug development process; drug submission requirements; ICH and FDA/EMEA/ROW guidelines.
- Some UNIX familiarity; R and imaging/genomics software packages.
Job Level: Professional
Compensation & Benefits
- Base compensation range: $95,000–$130,000.
- Benefits include medical/dental/vision/life, fitness reimbursement, short-/long-term disability, paid vacation (min 15 days + end-of-year shutdown), paid holidays, sick time, paid maternity/parental leave, 401(k) match, employee stock purchase plan, tuition reimbursement (up to $10,000/year), and Employee Resource Groups.
About This Role
The Senior Analyst, Statistical Programming leads and oversees statistical programming activities (internally and via vendors) to apply data standards; produce analysis datasets and specifications (CDISC ADaM); create tables, listings, figures, electronic submission components, and ad hoc analyses. Partners with Biostatistics to deliver submission-ready outputs; provides input to the Portfolio Lead (PL) on study timelines, milestones, issue escalation, and resource needs. Leads study teams of statistical programmers, provides vendor communication/quality oversight, and represents Statistical Programming as a functional lead. Helps implement the Data Strategy and develops standard programming practices across studies.
What You’ll Do
- Lead, coordinate, and manage statistical programming deliverables (creation, review, completion, delivery).
- Author CDISC ADaM analysis dataset specifications; define/document endpoint algorithms.
- Manage end-to-end programming from CRF data to electronic submission; ensure compliance with submission standards.
- Serve as Statistical Programming Lead to achieve study milestones.
- Verify consistency and proper use of data, analysis, and submission standards.
- Inform team members on programming requirements, deliverable status, and resourcing.
Who You Are
Senior Analyst with strong statistical programming skills, attention to detail, and ability to manage competing priorities.
Required Skills
- Bachelor’s degree.
- 5+ years relevant data management/analysis experience.
- 5+ years SAS Base; 5+ years SAS STAT/GRAPH/MACRO.
- 5+ years relevant industry experience; 5+ years clinical trial experience; 3+ years clinical database experience.
- CDISC and/or submissions experience.
- Knowledge of drug development process; drug submission requirements; ICH and FDA/EMEA/ROW guidelines.
- Some UNIX familiarity; R and imaging/genomics software packages.
Job Level: Professional
Compensation & Benefits
- Base compensation range: $95,000–$130,000.
- Benefits include medical/dental/vision/life, fitness reimbursement, short-/long-term disability, paid vacation (min 15 days + end-of-year shutdown), paid holidays, sick time, paid maternity/parental leave, 401(k) match, employee stock purchase plan, tuition reimbursement (up to $10,000/year), and Employee Resource Groups.