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Manager, Clinical Data Reporting & Analytics

at Bristol Myers Squibb

Bristol Myers SquibbHyderabad - TS - INPosted 2026-06-22
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Job description

Working with UsChallenging. 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.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.The PAL reports to TA lead of CDSSR&ADegree Requirements:BS computer science/Math’s/Stats/Life Sciences, programming, data management, scientific or analytic disciplineExperience 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) processStrong 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 ShinyDomain 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 systemThorough 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.Collaboration: Working well in a team environment, collaborating with cross-functional teams, stakeholders, and subject matter experts to gather requirements, share insights, and drive data-driven decision-making.Time management: Prioritizing tasks, managing deadlines, and handling multiple projects simultaneously, ensuring timely delivery of high-quality work.Adaptability: Being flexible and open to change, quickly adapting to new technologies, tools, and methodologies in the rapidly evolving field of data analysis.Curiosity and continuous learning: Having a natural curiosity to explore data, learn new techniques, and stay updated with the latest trends and advancements in data analysis, seeking opportunities for professional growth and development.Business acumen: Understanding the business context and objectives behind data analysis, aligning insights with organizational goals, and providing actionable recommendations to drive business outcomes.Ethical mindset: Demonstrating integrity and ethical behavior in handling sensitive data, ensuring compliance with data privacy regulations, and maintaining confidentiality.Travel
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