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Associate Director, Taip Principal Analyst

Bristol Myers Squibb
6-8 years
Not Disclosed
Hyderabad
1 June 3, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Director, TAIP Principal Analyst – Trial Analytics, Insights & Planning (TAIP)

Location: Hyderabad, Telangana, India
Company: Bristol Myers Squibb (BMS)
Department: Trial Analytics, Insights & Planning (TAIP)

Position Summary

The TAIP Principal Analyst is a mid-to-senior level position within the Trial Analytics, Insights & Planning (TAIP) organization at Bristol Myers Squibb. TAIP functions as an internal consulting team focused on accelerating clinical development through advanced analytics, strategic trial planning, and data-driven decision-making.

In this role, you will lead end-to-end analytics delivery for one or more global clinical trials while managing a project team of 3–5 Analysts and Senior Analysts. As a key analytics partner embedded within study teams, you will translate clinical trial requirements into actionable analytical strategies, oversee forecasting and feasibility assessments, and support informed decision-making throughout the trial lifecycle.

The role requires a strong understanding of clinical trial science, operational analytics, forecasting methodologies, and study optimization strategies. You will collaborate closely with cross-functional stakeholders and contribute to the successful execution of global clinical development programs.


Key Responsibilities

Clinical Trial Analytics Leadership

  • Lead study-level analytics planning and execution from protocol development through trial completion.

  • Manage and mentor a project team of 3–5 Analysts and Senior Analysts, ensuring high-quality and timely delivery of analytics outputs.

  • Translate study objectives into analytical workstreams including feasibility assessments, enrollment forecasting, site scoring, and performance monitoring.

  • Ensure consistency, scalability, and quality across analytical methodologies, assumptions, tools, and deliverables.

Strategic Trial Planning and Optimization

  • Develop and implement analytics strategies that support trial design, planning, and execution.

  • Conduct study optimization analyses including patient burden assessments, site burden evaluations, and competitive trial landscape reviews.

  • Support country allocation strategies and protocol design decisions through cost and operational analyses.

  • Identify opportunities to accelerate trial execution using data-driven insights.

Cross-Functional Collaboration

  • Partner with Clinical Operations, Feasibility, Therapeutic Area Leads, Clinical Development Teams, and other stakeholders.

  • Coordinate with field-based teams to integrate local market intelligence into feasibility and site selection strategies.

  • Support clinical supply planning through forecasting and operational analytics.

  • Communicate analytical findings and recommendations to study leadership and decision-makers.

Data Analytics and Insights

  • Utilize advanced analytics platforms and tools to generate actionable insights.

  • Analyze clinical trial data, enrollment metrics, site performance indicators, and operational trends.

  • Develop dashboards, reports, forecasting models, and analytical frameworks to support trial execution.

  • Apply critical thinking and evidence-based approaches to solve complex business and operational challenges.

Risk Management and Decision Support

  • Identify potential risks impacting study timelines, enrollment, or execution.

  • Escalate critical issues and propose mitigation strategies.

  • Deliver strategic recommendations that improve trial efficiency and effectiveness.


Required Qualifications

Education

  • Advanced degree preferred (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant discipline.

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

Experience

  • 6–8+ years of experience in clinical analytics, trial strategy, management consulting, clinical operations, or related healthcare analytics functions.

  • Experience supporting clinical trial delivery and operational decision-making.

  • Demonstrated experience leading projects and cross-functional teams.

  • Strong understanding of clinical development processes and study execution.