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.

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 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.

Qualification 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 Skills

• Good understanding the various clinical data sources such as EDC, Central lab, Local Lab, Medical Imaging, IVRS/IRT, ECG, CTMS and so on…
• Knowledge of CDISC standards (SDTM domains), with additional advantage if worked on SDTM transformations.
• Therapeutic Area knowledge in the clinical domain.
• Must be capable of reading and understanding a clinical trial protocol and collaborating with the clinical trial team in understanding the reporting needs.
• Good understanding of the clinical study database design in RAVE/Veeva/Oracle Clinical and /or any other study design EDC system
• Thorough understanding of Drug Discovery process and regulatory requirements (ICH, FDA, …)

Soft Skills

• Analytical thinking: The ability to think critically and analyze complex data sets, identifying patterns, trends, and insights to solve problems and make data-driven decisions with some guidance from seniors.
• Attention to detail: Must be attentive to the details during the requirements gatherings and effective communication of the actions and effective follow up thus ensuring accuracy and precision in data interpretation and reporting.
• Communication skills: Effectively conveying complex technical concepts and findings to both technical and non-technical stakeholders, including presenting data visually and using storytelling techniques to make data more accessible and understandable.
• Problem-solving: Applying logical reasoning and creative thinking to identify and resolve data-related issues, finding innovative solutions to improve data quality, analysis processes, and reporting. If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol Responsibilities BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People With Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california\-residents/

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