Senior Trial Analytics & Planning Analyst - Internal

Bristol-Myers Squibb; United States; On-site; USD 19,000 - 32,000; Full time

Job summary

Bristol Myers Squibb seeks a Senior Analyst for TAIP to advance trial analytics, forecasting, and planning within a global, cross-functional setting. You will contribute to enrollment forecasting, feasibility analyses, and protocol analytics while developing domain expertise over time.

The role embeds you in a clinical trial team, delivering high-quality analytics that accelerate drug development and improve study design.

Qualifications

• 3–6+ 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.

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 TAIP colleagues.
• Work within a specific clinical trial context, gaining exposure to operational strategy and protocol logic.
• Build therapeutic area knowledge over time to support targeted analyses.
• Ensure accuracy, consistency, and clarity in data models, dashboards, and insights for the study team.
• Collaborate across geographies, coordinating with analysts globally.
• 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 and communicate data-driven insights.

Skills

Communication

Structured problem-solving

MS Office

Education

Advanced degree

Tools

MS Office

Job description

Bristol Myers Squibb seeks a Senior Analyst for TAIP to advance trial analytics, forecasting, and planning within a global, cross-functional setting. You will contribute to enrollment forecasting, feasibility analyses, and protocol analytics while developing domain expertise over time.

The role embeds you in a clinical trial team, delivering high-quality analytics that accelerate drug development and improve study design.