Bristol Myers Squibb
Pharmaceutical
Manager,ProgrammingAnalyticsLead
Neural analysis suggests this role is
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“Manager, Programming Analytics Lead at Bristol Myers Squibb. Skills: SAS, Qlik, SQL/PLSQL, reporting, analytics. Serve as primary point of contact. Collaborate with clinical stakeholders”
What You'll Achieve.
driving efficient and effective reporting and analytics solutions; ensuring a "first time right" approach; ensuring patient safety; efficient report delivery; improve data quality; analysis processes; reporting
Industry & Context.
Analytical thinking; Problem-solving; Applying logical reasoning; creative thinking; identify and resolve data-related issues
Flexible to work with global stakeholders across different time zones
What They're Looking For.
Must Have
BS computer science/Math’s/Stats/Life Sciences, programming, data management, scientific or analytic discipline, 5+ years’ experience in the development of reporting and analytics in the Pharmaceutical Industry with a focus on clinical trials, SAS, Qlik, SQL/PLSQL, SDLC (Software Development Life Cycle) process, understanding of relational databases, ETL concepts
Nice to Have
elluminate Mapper, JReview, Spotfire, Tableau, Power BI, Micro Strategy, Yellowfin, Python (NumPy and Pandas), R, R Shiny, CDISC standards (SDTM domains), worked on SDTM transformations, Therapeutic Area knowledge in the clinical domain, reading and understanding a clinical trial protocol, clinical study database design in RAVE/Veeva/Oracle Clinical, any other study design EDC system
What You'll Do.
Serve as primary point of contact
Collaborate with clinical stakeholders
Translate requirements into specifications
Develop reports and analytics visualizations
Test developed reports
Adhere to documentation and process compliance
Analyse clinical trial needs
Negotiate with stakeholders
Prioritize deliverables
Demonstrate technical expertise
Work cohesively with team members
Keeping up to date with new reporting tools
Ensure compliance with procedures
Contribute to other sub-functions
Flexible to work with global stakeholders
How You'll Work.
Team & Collaboration
Collaborate with clinical stakeholders; Work cohesively with team members; embracing feedback and suggestions
Communication Scope
Effectively conveying complex technical concepts; presenting data visually; using storytelling techniques
Process & Methodology
Prioritize deliverables based on business criticality, seek assistance when needed
Full Job Description
**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: [careers.bms.com/working-with-us](https://careers.bms.com/working-with-us). The PAL Manager SRD, CDR&A is a key individual contributor responsible for managing multiple studies across various Therapeutic Areas. This role will serve as the primary point of contact for stakeholders, taking ownership of the entire report development and delivery process. This includes gathering reporting and analytics requirements, utilizing tools and programming languages such as SAS, elluminate Mapp, and Qlik to develop reports, and ensuring adherence to defined processes, timelines, and deliverable quality standards. The PAL Manager will play a crucial role in driving efficient and effective reporting and analytics solutions for our organization. _**Key Responsibilities:**_ Serve as the primary point of contact for multiple studies in different Therapeutic Areas. Collaborate with clinical stakeholders to understand their reporting and analytics needs aligned with study protocols. Translate requirements into comprehensive reporting development specifications. Utilize standard reports whenever possible and to suggest
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