Serves as a point of contact for the assigned study.
Designing, developing, and implementing complex custom reports using various clinical data management 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.
Requirements
Expert in clinical data review listings and analytics and use data to drive key business decisions. Willing to learn new technological skills and work through collaboration.
Required Skills
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 Clinical 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 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 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.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being ; including, but not limited to:
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
Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. A
Benefits
Dental insuranceVision insurance401(k)Paid time offEquity / stock optionsPerformance bonusParental leave
Additional Information
About This Role
The Senior Clinical Data Management 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 clinical data management 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.
Biogen · Research Triangle Park, NC