Senior Report Developer

About This Role

The Senior Report Developer is responsible for the development and maintenance reports for use in clinical trials, load data from various sources into data warehouse, program custom mappings and develop custom visualizations for ongoing data review. This Role will be responsible for the development of Standard Reports catalogue (e.g. exception listings, clean patient tracker etc.) 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, 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.

• 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 Mangers in specification development for Data Review Listings.

• Minimum 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.

• SAS, R and Python

• 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