Senior Analyst I Trial Analytics, Insights & Planning TAIP

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, 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:

o 3 6+ years of experience in consulting, healthcare analytics, life sciences strategy, or clinical trial planning and delivery is required

o Proven ability to manage and deliver complex analytical projects in fast-paced environments

Skills:

o Excellent communication and structured problem-solving skills

o Strong MS Office (Excel, PowerPoint) skills required

o Interest in developing deeper expertise in therapeutic areas and clinical trial analytics