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Senior Analyst I

Bristol Myers Squibb
3-6 years
Not Disclosed
Hyderabad
1 June 3, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding

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

Location: Hyderabad, Telangana, India
Job Requisition ID: R1599684
Company: Bristol Myers Squibb (BMS)

Position Summary

The Senior Analyst I – Trial Analytics, Insights & Planning (TAIP) role offers an opportunity for professionals with experience in consulting, healthcare analytics, life sciences strategy, or clinical trial operations to contribute directly to the acceleration of global drug development.

As part of Bristol Myers Squibb's Trial Analytics, Insights & Planning (TAIP) organization, you will work within an internal consulting model focused on delivering data-driven insights that improve clinical trial planning and execution.

Senior Analysts are aligned to one of two development tracks:

Analytical Track

Focus areas include:

  • Enrollment forecasting

  • Data modeling

  • Dashboard development

  • Site performance analytics

  • Operational reporting

Scientific Track

Focus areas include:

  • Protocol analysis

  • Patient population sizing

  • Eligibility criteria assessment

  • Trial feasibility planning

  • Clinical study strategy

While analysts may specialize in one track initially, exposure to both scientific and analytical domains is encouraged to build comprehensive expertise over time.

Working within a dedicated clinical trial team, you will support key analytics workstreams that enable smarter, faster, and more effective trial execution.


Key Responsibilities

Clinical Trial Analytics

  • Own and deliver key trial-level analytics workstreams, including enrollment forecasting, feasibility analyses, and protocol assessments.

  • Translate study requirements into structured analytical outputs in collaboration with senior TAIP team members.

  • Support clinical trial planning and execution through data-driven insights and recommendations.

  • Develop forecasting models, reports, dashboards, and analytical tools to support study teams.

Study Optimization and Strategic Analysis

  • Analyze site performance, patient burden, enrollment trends, and competitive trial landscapes.

  • Support optimization efforts related to study design, country allocation, and operational trade-offs.

  • Contribute to cost analyses and strategic planning initiatives.

  • Integrate external and field-based insights into feasibility and trial planning activities.

Data Analysis and Reporting

  • Utilize trial analytics platforms and reporting tools to generate actionable insights.

  • Ensure the accuracy, consistency, and quality of analytical deliverables.

  • Present findings in a clear and structured manner to stakeholders and study teams.

  • Support analytics that may impact clinical supply planning and site-level operational requirements.

Cross-Functional Collaboration

  • Work closely with global team members across multiple geographies and time zones.

  • Collaborate with Clinical Operations, Feasibility, Trial Strategy, and Therapeutic Area teams.

  • Support project execution through effective communication and coordination.

Critical Thinking and Problem Solving

  • Analyze complex datasets and operational challenges.

  • Challenge assumptions and identify opportunities for improvement.

  • Develop evidence-based recommendations that support strategic decision-making.


Qualifications

Education

Preferred:

  • MSc

  • MPH

  • PharmD

  • PhD

  • MBA

  • Other relevant advanced degree

Required:

  • Bachelor's degree in Life Sciences, Pharmacy, Public Health, Statistics, Data Analytics, Business, or a related field.


Experience

  • 3–6+ years of experience in one or more of the following areas:

    • Management Consulting

    • Healthcare Analytics

    • Life Sciences Strategy

    • Clinical Trial Planning

    • Clinical Operations

    • Clinical Research

    • Pharmaceutical Analytics

  • Experience managing and delivering complex analytical projects.

  • Exposure to clinical development or clinical trial environments is preferred.

  • Ability to work effectively in fast-paced, cross-functional environments.