Senior Report Developer

Overview

The 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. This role will develop a standard reports catalogue (e.g., exception listings, clean patient tracker) used for data review and reconciliations by the DM Operations staff and oversee automation projects such as workflow for common data management programming and validation purposes.

Serves as a point of contact for the assigned study, attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive feedback. The candidate keeps project management informed of any issues that might impact project target dates, scope, and escalates potential problems effectively and timely, balances multiple task assignments, communicates needs to the supervisor for needed resources, and mentors FSP programmers as needed.

• Serve as a 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.

Expert in data review listings and analytics who uses data to drive key business decisions, willing to learn new technological skills and work collaboratively.

• Minimum 3+ years of industry experience in report and visualization development using tools or platforms such as Elluminate, SAMA, Spotfire, Qlik, Tableau, working in the biotechnology or pharmaceutical industry.
• Strong SQL skills in a clinical data management environment.
• In‑depth knowledge of visualization design and 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 and proven ability to manage multiple, competing priorities.
• Experience working in a matrix environment and collaborating across functions and organizations, with 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.

• SAS, R, and Python.

Job Level: Professional

The base compensation range for this role is: $93,000.00‑$. Base salary is determined through an analytical approach utilizing a combination of factors including relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive short‑term and long‑term incentives, including cash bonus and equity incentive opportunities.

• Medical, Dental, Vision, and Life insurance
• Fitness & Wellness programs including fitness reimbursement
• Short‑ and Long‑Term Disability insurance
• Minimum 15 days of paid vacation and 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 up to $10,000 per calendar year
• Employee Resource Groups participation

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.