Senior Report Developer

About This Role Senior Report Developer is responsible for the development and maintenance of reports for use in clinical trials, loading data from various sources into a data warehouse, programming custom mappings, and developing custom visualizations for ongoing data review. The role manages the Standard Reports catalog—including exception listings, clean patient trackers, and other data review and reconciliation reports for DM Operations staff—and leads automation projects such as workflow development for common data‑management programming and validation purposes. Serves as the primary point of contact for assigned projects, attends meetings, drives analytical problem solving, focuses on deliverables, and provides constructive feedback. Reports any issues that may impact project timelines or scope and escalates potential problems effectively. Balances multiple task assignments and communicates needs to obtain necessary resources, while mentoring FSP programmers as needed. What You’ll Do Serve as the point of contact for the assigned study. Design, develop, and implement complex custom reports using various data sources. Load data from various sources into the data warehouse, program custom mappings, and develop custom visualizations for ongoing data review. Attend meetings, participate in discussions, use an analytical approach to problem solving, focus on deliverables, and provide constructive feedback. Support Data Review Study Implementation by following the planned implementation of real‑time data visualization solutions. Provide support in handling system upgrades and user access management. Leverage technical expertise to define feasible solutions and drive strategic use and implementation of new reports/visualizations, including any applicable training material. Support continuous process improvement initiatives for development and validation of tasks related to reports and other clinical applications. Provide support to Data Managers in specification development for Data Review Listings. Who You Are Expert in data review listings and analytics who uses data to drive key business decisions, is willing to learn new technological skills, and works effectively through collaboration. Required Skills Minimum of 3+ years of industry experience in reports and visualization development using tools or platforms such as Elluminate, SAMA, Spotfire, Qlik, Tableau, within the biotechnology or pharmaceutical industry. Strong SQL skills working in a clinical data management environment. In‑depth knowledge of visualization design and a good understanding of end‑to‑end data flow in data management. Strong technical experience with data management reports and listings such as Clean Patient Tracker, DM Metrics, coding listings, etc. High attention to detail, including a proven ability to manage multiple competing priorities. Experience working in a matrix environment and collaborating across functions and organizations, including demonstrated ability to influence without authority. Knowledge of GCP and other regulations, good knowledge of CDISC, SDTM standards. Excellent written and oral communication skills, demonstrated leadership, problem‑solving, conflict resolution, and team‑building skills. Preferred Skills SAS, R, and Python Job Level Professional Additional Information The base compensation range for this role is $93,000.00–$121,000.00. Base salary is determined through an analytical approach that considers relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short‑term and long‑term incentives, including cash bonuses 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, and 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 Equal Employment Opportunity 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 SupportFinity™