Sr Analyst, Statistical Programming

About this role

This is a hybrid position that requires in‑person workdays at our offices. The position is based in either Durham, NC or Cambridge, MA.

The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally through vendors. Responsibilities include applying data standards, producing analysis datasets, drafting analysis dataset specifications, creating tables, listings, figures, electronic submission components, and performing ad‑hoc analyses.

• Lead, coordinate, and manage timely creation, oversight, review, completion, and delivery of statistical programming activities and deliverables.
• Author CDISC ADaM analysis dataset specifications and identify potential data issues or critical data examination areas.
• Work with statistics on defining and documenting programming endpoint algorithms across a study and, where applicable, contribute to therapeutic area‑level algorithms.
• Manage end‑to‑end programming of deliverables from CRF collections through electronic submission, including preparation of electronic submission components.
• Serve as the Statistical Programming Lead to achieve study milestones and collaborate with the Portfolio Lead, study manager, and other stakeholders on issues and resource needs.
• Verify program consistency and usage of data, analysis, and submission standards within a study in consultation with data standards, statistical submissions management, and the data strategy plan.
• Inform internal and external project team members of statistical programming requirements, deliverable status, and resource needs.

• Bachelor’s degree required.
• 5+ years relevant work experience within an organization focused on data management and analysis.
• 5+ years SAS Base programming and 5+ years using SAS STAT, GRAPH, and MACRO.
• 5+ years relevant industry experience and 5+ years clinical trial experience.
• 3+ years clinical database experience.
• CDISC and/or submissions experience.
• Knowledge of drug development process, clinical trials, drug submission requirements, and relevant ICH, FDA/EMEA/ROW guidelines.
• Some familiarity with UNIX and software development packages (e.g., R, imaging and genomics software packages).
• Strong statistical programming skills with attention to detail and the ability to manage competing priorities.

• Base salary range: $95,000–$130,000.
• Short‑term and long‑term incentives, including cash bonus and equity opportunities.
• Extensive benefits: medical, dental, vision, life insurance, fitness and wellness programs, short‑ and long‑term disability insurance.
• Paid vacation: minimum 15 days, plus end‑of‑year shutdown time off (Dec
  26–Dec
  31), up to 12 company‑paid holidays, and 3 paid days off for personal significance.
• Paid sick time: 80 hours per calendar year.
• Paid maternity and parental leave.
• 401(k) program with company match, employee stock purchase plan, and tuition reimbursement up to $10,000 per year.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law.

Biogen is an E‑Verify Employer in the United States.