Sr. Analyst, Statistical Programming
Biogen
August 21, 2026
Remote friendly (Cambridge, MA)
United States
Clinical Research and Development
Role Responsibilities:
- Lead, coordinate, and manage timely creation, oversight, review, completion, and delivery of statistical programming activities and deliverables.
- Author CDISC ADaM analysis data set specifications; identify potential data issues and define/document programming endpoint algorithms.
- Manage end-to-end programming from CRF collections through electronic submission, including preparation of electronic submission components; ensure compliance to submission standards with SMEs.
- Serve as Statistical Programming Lead to achieve study milestones; collaborate with Portfolio Lead/manager on issues and resource needs.
- Verify program consistency and usage of data, analysis, and submission standards.
- Inform project team members of programming requirements, deliverable status, and resource needs.
Qualifications/Required Skills:
- Bachelor’s degree.
- 5+ years relevant work experience in data management and analysis.
- 5+ years SAS Base programming with 5+ years using SAS STAT, GRAPH, and 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 and clinical trials.
- Knowledge of drug submission requirements and relevant ICH and FDA/EMEA/ROW guidelines.
- Some familiarity with UNIX and software development packages (R, imaging, and genomics software).
Benefits/Compensation (as stated):
- Base compensation range: $95,000.00–$130,000.00.
- Medical, Dental, Vision, Life; fitness reimbursement; short- and long-term disability; paid vacation (minimum 15 days) plus end-of-year shutdown; paid holidays and personal days; sick time; maternity/parental leave; 401(k) match; employee stock purchase plan; tuition reimbursement up to $10,000/year; Employee Resource Groups participation.
- Lead, coordinate, and manage timely creation, oversight, review, completion, and delivery of statistical programming activities and deliverables.
- Author CDISC ADaM analysis data set specifications; identify potential data issues and define/document programming endpoint algorithms.
- Manage end-to-end programming from CRF collections through electronic submission, including preparation of electronic submission components; ensure compliance to submission standards with SMEs.
- Serve as Statistical Programming Lead to achieve study milestones; collaborate with Portfolio Lead/manager on issues and resource needs.
- Verify program consistency and usage of data, analysis, and submission standards.
- Inform project team members of programming requirements, deliverable status, and resource needs.
Qualifications/Required Skills:
- Bachelor’s degree.
- 5+ years relevant work experience in data management and analysis.
- 5+ years SAS Base programming with 5+ years using SAS STAT, GRAPH, and 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 and clinical trials.
- Knowledge of drug submission requirements and relevant ICH and FDA/EMEA/ROW guidelines.
- Some familiarity with UNIX and software development packages (R, imaging, and genomics software).
Benefits/Compensation (as stated):
- Base compensation range: $95,000.00–$130,000.00.
- Medical, Dental, Vision, Life; fitness reimbursement; short- and long-term disability; paid vacation (minimum 15 days) plus end-of-year shutdown; paid holidays and personal days; sick time; maternity/parental leave; 401(k) match; employee stock purchase plan; tuition reimbursement up to $10,000/year; Employee Resource Groups participation.