Senior Clinica Data Management Report Developer

About This RoleThe 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 be responsible for the development of the Standard Reports catalogue (e.g., exception listings, clean patient tracker) used for data review and reconciliations by the DM Operations staff and is responsible for some automation projects such as workflow for common data management programming and validation purposes. Serves as a point of contact for the assigned project. Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive feedback. Keeps those responsible for project management informed of any issues that might impact project target dates or scope, and escalates potential problems effectively and in a timely manner. Balances multiple task assignments and communicates needs to supervisor to obtain needed resources. Mentors FSP programmers as needed.What You'll DoServes as a point of contact for the assigned study.Designing, developing, and implementing complex custom reports using various data sources.Load data from various sources into 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: follows the planned implementation of real time data visualization solution.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 AreExpert in data review listings and analytics and use data to drive key business decisions. Willing to learn new technological skills and work through collaboration.Required SkillsMinimum of 3+ years industry experience in reports and visualization development using tools or platforms such as Elluminate, SAMA, Spotfire, Qlik, Tableau, working in the biotechnology or pharmaceutical industry.Strong SQL skills working in the 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 including 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 SkillsSAS, R and PythonAdditional InformationThe base compensation range for this role is: $93,000.00-$121,000.00Base 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 your future potential based on individual, business unit and company performance.BenefitsMedical, Dental, Vision, & Life insurancesFitness & Wellness programs including a fitness reimbursementShort- and Long-Term Disability insuranceA 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 Significance80 hours of sick time per calendar yearPaid Maternity and Parental Leave benefit401(k) program participation with company matched contributionsEmployee stock purchase planTuition reimbursement of up to $10,000 per calendar yearEmployee Resource Groups participationWhy Biogen?We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.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