Sr. Analyst, Statistical Programming

About This Role The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components, and ad hoc analyses. You will partner with Biostatistics to deliver high quality, submission‑ready statistical outputs with some supervision. You are responsible for providing input to the Portfolio Lead (PL) on overall study timeline, monitoring and meeting agreed‑upon study milestones, escalating issues as needed to their PL counterpart and estimating resources needs. You will lead a study team of statistical programmers to accomplish tasks and communicate issues, as necessary, to line management. This includes communication and quality oversight of the vendor. You will represent the Statistical Programming perspective to the study team and is often the sole functional representative. You will help to implement the Data Strategy, provide input to the Data Strategy Lead and DM lead on the strategic direction of the study to ensure appropriate statistical programming standards implementation and serve as reference for the study to the Data Sharing representative. You will develop and implement standard programming practices while also ensuring that they are employed across a study. You will collaborate with technical programming on tools and process improvement for Statistical Programming. This is a hybrid position that requires in-person workdays at our facilities in Cambridge, MA. What You’ll Do Lead, coordinate and manage timely creation, oversight, review, completion, and delivery of statistical programming activities and deliverables of projects. Author CDISC ADaM analysis dataset specifications including the identification of potential data issues or areas of critical data examination. Work with statistics on defining and documenting programming endpoint algorithms across a study, drug program and/or contributing to TA level algorithms. Manage the end‑to‑end programming of deliverables from CRF collections through electronic submission including preparation of electronic submission components; work with SMEs to ensure compliance to submission standards. Serve as the Statistical Programming Lead to achieve milestones for a study; collaborate with PL and/or manager on issues or 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. Who You Are You are a Senior Analyst with strong statistical programming skills who pays close attention to detail and has the proven ability to manage some competing priorities. Required Skills Bachelor’s degree required. 5+ years relevant work experience within an organization with a focus on 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, relevant ICH and FDA/EMEA/ROW guidelines. Some familiarity with UNIX as well as software development packages (R, imaging and genomics software packages). Additional Information The base compensation range for this role is: $100,000.00-$130,000.00. Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short‑term and long‑term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize future potential based on individual, business unit, and company performance. Benefits Medical, Dental, Vision, & Life insurances Fitness & Wellness programs including a fitness reimbursement Short- and long‑term Disability insurance A minimum of 15 days of paid vacation and an additional end‑of‑year shutdown time off (Dec 26-Dec 31) Up to 12 company paid holidays + 3 paid days off for Personal Significance 80 hours of sick time per calendar year Paid Maternity and Parental Leave benefit 401(k) program participation with company matched contributions Employee stock purchase plan Tuition reimbursement of up to $10,000 per calendar year Employee Resource Groups participation Job Level: Professional. 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. #J-18808-Ljbffr Biogen