Manager, Programming Analytics Lead

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 . 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.

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 solutions. Develop reports and analytics visualizations according to specified requirements, ensuring a "first time right" approach. Test developed reports, document results, and provide peer review support as needed. Adhere to documentation and process compliance, notifying management of any noncompliance. Analyse clinical trial needs holistically to determine effective monitoring approaches and ensure patient safety. Negotiate with stakeholders and foster collaboration for efficient report delivery. Prioritize deliverables based on business criticality and seek assistance when needed. Demonstrate technical expertise to develop solutions for complex reporting needs. Work cohesively with team members, embracing feedback and suggestions. Keeping up to date with new reporting tools, techniques, and industry trends to enhance skills and knowledge. Ensure compliance with procedures, trainings, and policies defined by the organization. Contribute to other sub-functions of CDR&A as needed to support business priorities. Flexible to work with global stakeholders across different time zones while ensuring business continuity.

Degree Requirements: BS computer science/Math’s/Stats/Life Sciences, programming, data management, scientific or analytic discipline Experience Requirements: 5+ years’ experience in the development of reporting and analytics in the Pharmaceutical Industry with a focus on clinical trials. Key Competency Requirements: Primary technical Skills: Experience with various reporting and analytic tools like SAS, Qlik, SQL/PLSQL and added advantage, if experienced in eClinical tool elluminate Mapper. Hands on experience in SDLC (Software Development Life Cycle) process Strong understanding of relational databases and ETL concepts. Secondary Technical skills: Good to have hands on/Knowledge of JReview, Spotfire, Tableau, Power BI, Micro Strategy, Yellowfin or any visualization development tool and /or programming languages such as Python (NumPy and Pandas), R and R Shiny Domain