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Senior Report Developer

Biogen
Remote friendly (Triangle, NC)
United States
$93,000 - $121,000 USD yearly
IT

Role Summary

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 contribute to the development of a Standard Reports catalogue (e.g., exception listings, clean patient tracker) used for data review and reconciliations by DM Operations staff and will drive automation projects for data management programming and validation. The position serves as a point of contact for the assigned project, participates in meetings, and supports problem solving, deliverables, and escalation of issues in a timely manner. Mentors FSP programmers as needed.

Responsibilities

  • Serves 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.
  • Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive feedback.
  • Supports Data Review Study Implementation: follows the planned implementation of real time data visualization solution.
  • Provides support in handling system upgrades, 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.
  • Supports continuous process improvement initiatives for development and validation of tasks related to Reports and other clinical applications.
  • Provides support to Data Managers in specification development for Data Review Listings.

Qualifications

  • Required: Minimum of 3+ years industry experience in reports and visualization development using tools or platforms such as Elluminate, SAMA, Spotfire, Qlik, Tableau, in the biotechnology or pharmaceutical industry.
  • Required: Strong SQL skills in a clinical data management environment.
  • Required: In-depth knowledge of Visualization Design and understanding of end-to-end data flow in Data Management.
  • Required: Technical experience with Data Management Reports and Listings (e.g., Clean Patient Tracker, DM Metrics, coding listings).
  • Required: High attention to detail and ability to manage multiple priorities.
  • Required: Experience in a matrix environment with cross-functional collaboration and influence without authority.
  • Required: Knowledge of GCP and regulations; good knowledge of CDISC, SDTM standards.
  • Required: Excellent written and oral communication skills; demonstrated leadership, problem solving, conflict resolution, and team-building abilities.
  • Preferred: SAS, R and Python.

Skills

  • Data review listings and analytics
  • Analytical problem solving and data-driven decision making
  • Communication and collaboration across functions