Senior Analyst, Trial Analytics, Insights & Planning (TAIP)
Bristol Myers Squibb•Warszawa
Widełki nieujawnione
⭐ Nieznany📄 other
📝 Opis główny / Wstęp
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 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:
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
Compensation Overview
Warsaw - PL: zł271,580 - zł329,085
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.
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
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 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.
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, challenge assumptions, and generate strategic, evidence-based recommendations
- Education: Preferred advanced degree (e.g., MSc, MPH, PharmD, PhD, MBA) in a relevant field
- 3+ years of experience in consulting, healthcare analytics, life sciences strategy, or clinical trial planning and delivery is required
- Proven ability to manage and deliver complex analytical projects in fast-paced environments
- Excellent communication and structured problem-solving skills
- Strong MS Office (Excel, PowerPoint) skills required
- Interest in developing deeper expertise in therapeutic areas and clinical trial analytics
- Grow in a Learning Environment: Build your scientific, analytical, and strategic expertise over time
- Be Part of an Internal Consulting Model: Operate in a pod-based team inspired by top-tier strategy firms
- Progress Through a Clear Career Path: Advance through a structured path modeled on strategic consulting, with transparent expectations, ~2-3 years per role, and rapid progression based on ownership and impact
- Pathway to Strategic Leadership at BMS: Career development is actively encouraged and expected, with opportunities to move into broader strategy and leadership roles within BMS in a short timeframe
- Accelerate Therapies to Patients: Help drive clinical decisions that bring treatments to patients faster
Compensation Overview
Warsaw - PL: zł271,580 - zł329,085
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.
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
📡 Metadata statystyk
Źródłolinkedin
Slug / IDlinkedin-senior-analyst-trial-analytics-insights-planning-taip-at-bristol-myers-squibb-4368648054
Opublikowano19 marca 2026
Wygasa—
Pobranie (Ingest)24 marca 2026
🗂 Szczegóły oferty
📋 Informacje
LokalizacjaWarszawa
Tryb pracy—
Etat—
DoświadczenieNieznany
Min. lat doświadczenia6+
Typ kontraktuOther
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