About This Role
The Senior Clinica 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.
What You’ll Do
- 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.
Who You Are
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
Additional Information
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. 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.
Biogen Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Biogen and has not been reviewed or approved by Biogen.
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Fair & Transparent Compensation — Pay is generally positioned as competitive and often perceived as fair across roles, with total compensation framed as strong when bonus and equity are included. Compensation sentiment is described as above-average overall, though it varies by function and business cycle.
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Equity Value & Accessibility — Equity programs are repeatedly highlighted as a meaningful part of the total package, including stock programs and an employee stock purchase plan. Equity and bonus elements are portrayed as important contributors to feeling well rewarded beyond base pay.
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Leave & Time Off Breadth — Time-off benefits are described as distinctive, including a year-end shutdown and a paid sabbatical after extended tenure. Vacation, holidays, sick time, and personal-significance days are also presented as supportive of work-life needs.
Biogen Insights
What We Do
Through cutting-edge science and medicine, Biogen discovers, develops and delivers innovative therapies worldwide for people living with serious neurological and neurodegenerative diseases. Founded in 1978, Biogen is a pioneer in biotechnology and today the Company has the leading portfolio of medicines to treat multiple sclerosis, has introduced the first and only approved treatment for spinal muscular atrophy, and is at the forefront of neurology research for conditions including Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. Biogen also manufactures and commercializes biosimilars of advanced biologics. With approximately 7000 people worldwide, we are truly a global organization, headquartered in Cambridge, Massachusetts, which is also home to our research operations. Our international headquarters are based in Zug, Switzerland and we have world-class manufacturing facilities in North Carolina and Denmark. We offer therapies globally through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries. For more information, please visit www.biogen.com. Follow us on social media – Twitter, LinkedIn, Facebook, YouTube.
