Senior Analyst I - Trial Analytics, Insights & Planning (TAIP)

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 .

Title Senior Analyst – Trial Analytics, Insights & Planning (TAIP) Sr. Mgr level (EG 120) Location: Hyderabad --- Position Summary The Senior Analyst role in Bristol Myers Squibb’s Trial Analytics, Insights, and Planning (TAIP) unit is an excellent opportunity for professionals with approximately 3–6 years of experience in consulting, life sciences analytics, or clinical trial operations to step into an internal consulting environment that directly accelerates drug development. Senior Analysts join one of two tracks based on their background and preference: · The Analytical track focuses on forecasting, data modelling, dashboards, and site performance analytics. · The Scientific track focuses on protocol logic, patient population sizing, eligibility criteria, and feasibility planning. Regardless of track, you will gain exposure to both domains and are expected to develop strong, well-rounded expertise in scientific and analytical areas over time. As a Senior Analyst, you will be embedded in a specific clinical trial team and work under the guidance of more senior team members to deliver core analytics workstreams that support smarter, faster trial execution. This includes taking ownership of trial forecasting models, feasibility analyses, and protocol analytics — always with the goal of helping bring therapies to patients more effectively. You are not expected to be a therapeutic area or protocol expert on day one, but you will be expected to build domain knowledge over time, apply structured thinking to complex trial problems, and deliver high-quality, consistent outputs. You’ll also be part of a global, cross-functional team, working closely with peers across time zones to deliver with speed and precision. --- Key Responsibilities · Own key trial-level analytics workstreams (e.g., enrollment forecasting, feasibility analysis, protocol input) · Translate structured study requirements into analytical deliverables in collaboration with more senior TAIP colleagues · Work within a specific clinical trial context, gaining exposure to operational strategy, protocol logic, and real-world trial planning challenges · Build therapeutic area knowledge over time, contributing to more targeted and scientifically grounded analyses · Ensure accuracy, consistency, and clarity in data models, dashboards, and insights shared with the study team · Collaborate across geographies, coordinating with other analysts and team members globally · Contribute to cost-related analyses, such as country mix optimization and study design trade-offs · Support study optimization by analyzing site and patient burden, competitor activity, and external data sources · Coordinate with field-based colleagues to integrate local insights into feasibility and planning analytics · Utilize trial analytics platforms and tools to generate, structure, and communicate data-driven insights · Support analytics that may inform clinical supply forecasting or site-level supply considerations · Applies critical thinking to analyze complex data,