Analyst I- Trial Analytics, Insights & Planning (TAIP) at Bristol Myers Squibb

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

03 Jul, 26

Salary

0.0

Posted On

04 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical mindset, Data modeling, Forecasting, Clinical trial analytics, Excel, PowerPoint, Strategic decision-making, Structured problem-solving, Feasibility analysis, Communication skills, Attention to detail, Clinical research, Healthcare strategy, Data-driven insights, Cross-functional collaboration

Industry

Pharmaceutical Manufacturing

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. Position Title Analyst – Trial Analytics, Insights & Planning (TAIP) (EG-90) Location: HYD Position Summary The Analyst role is an entry-level position within Bristol Myers Squibb’s Trial Analytics, Insights, and Planning (TAIP) organization — an internal consulting team dedicated to accelerating clinical development through data-driven analytics and trial planning. As an Analyst, you will be embedded in a project-based delivery team supporting a specific clinical trial. You’ll work under the guidance of more senior team members to help execute feasibility analyses, forecasting models, dashboards, and other core analytics deliverables. You are not expected to be a clinical or therapeutic area expert at the start, but you will be expected to learn quickly, apply structured problem-solving, and contribute to real trial decisions from day one. This is an ideal role for recent graduates with an advanced degree and a strong analytical or scientific background who are ready to build hands-on experience at the intersection of data, clinical trials, and strategic decision-making. The Analyst position offers two tracks based on your background: The Analytical track focuses on forecasting, data modelling, dashboards, and trial performance analytics. The Scientific track focuses on protocol logic, patient population sizing, eligibility criteria, and feasibility support. While prior clinical trial experience is not required, we’re looking for candidates with a strong analytical mindset, curiosity, and the ability to connect data to strategic decisions that accelerate development. Key Responsibilities Support delivery of analytics for a specific clinical trial, contributing to feasibility, forecasting, and operational planning Execute structured analytics tasks using established tools, templates, and inputs under the guidance of senior team members Gain exposure to trial protocols and therapeutic area logic, developing domain knowledge over time Deliver high-quality, timely analytics outputs (e.g., site tiering, enrollment dashboards, patient population sizing) Collaborate with a global, cross-functional team, aligning with peers in different time zones and geographies Grow your skills across analytical, scientific, and strategic domains through active participation in delivery and internal capability-building 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, challenge assumptions, and generate strategic, evidence-based recommendations Qualifications & Experience Education: Preferred advanced degree (e.g., MSc, MPH, PharmD, PhD, MBA) in a relevant field Experience: 0–3+ years of experience in consulting, analytics, clinical research, or healthcare strategy Prior academic or internship exposure to clinical trial data or healthcare analytics is a plus Skills: Strong analytical mindset and attention to detail Proficiency in Excel and PowerPoint Strong written and verbal communication skills Curiosity, initiative, and a willingness to learn quickly in a collaborative team environment Why Join This Team? Learn by Doing: Contribute directly to global clinical trials and build real-world experience from day one Grow with Purpose: Develop the analytical and scientific capabilities needed to progress within TAIP Work in a Consulting-Style Team: Join a dynamic, project-based environment modeled after top-tier strategy firms Advance Through a Structured Career Ladder: Follow a transparent growth path with ~2–3 years at each level—designed to build toward strategic leadership roles within TAIP and across BMS Accelerate Therapies to Patients: Help bring life-changing treatments to patients through data-driven decision support 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 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/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1599690 : Analyst I- Trial Analytics, Insights & Planning (TAIP) Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.

Responsibilities

Support the delivery of clinical trial analytics, including feasibility, forecasting, and operational planning. Collaborate with global cross-functional teams to provide data-driven insights that accelerate clinical development.