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Associate Director, Taip Principal Analyst_Trial Analytics, Insights & Planning (Taip)

Bristol Myers Squibb
6-8 years
35-50 lakhs
Hyderabad
10 June 15, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Position Summary

The TAIP Principal Analyst is a mid-to-senior level role within BMS's Trial Analytics, Insights & Planning (TAIP) organization. This team functions as an internal consulting group focused on accelerating clinical development through advanced analytics, forecasting, strategic planning, and trial optimization.

The role is responsible for leading end-to-end analytics delivery for one or more global clinical trials while managing a team of Analysts and Senior Analysts. The individual serves as a strategic analytics partner to study teams, driving data-driven decision-making throughout the clinical trial lifecycle.


Key Responsibilities

Clinical Trial Analytics Leadership

  • Own study-level analytics planning and execution from protocol concept through trial completion.

  • Lead analytics strategy for one or more global clinical trials.

  • Ensure timely delivery of high-quality analytical outputs.

Team Management

  • Lead and mentor a team of 3–5 Analysts and Senior Analysts.

  • Manage workload, priorities, and project delivery.

  • Support team development and performance improvement.

Trial Planning & Forecasting

  • Develop and oversee:

    • Enrollment Forecasting

    • Site Selection & Scoring

    • Feasibility Analysis

    • Trial Performance Dashboards

    • Recruitment Analytics

Cross-Functional Collaboration

  • Partner with:

    • Clinical Operations

    • Feasibility Teams

    • Therapeutic Area Leads

    • Study Teams

    • Clinical Supply Teams

  • Act as the primary analytics advisor within trial teams.

Study Optimization & Strategic Insights

  • Analyze:

    • Patient Burden

    • Site Burden

    • Competitive Trial Landscape

    • Country Mix Optimization

    • Protocol Design Trade-offs

  • Recommend strategies to improve trial efficiency and execution.

Advanced Analytics & Reporting

  • Utilize analytics platforms and tools to generate insights.

  • Develop dashboards, reports, and forecasting models.

  • Support evidence-based decision-making through data visualization.

Risk Management

  • Identify execution risks proactively.

  • Escalate critical issues and recommend mitigation plans.

  • Use analytics to accelerate study timelines and improve outcomes.


Required Qualifications

Education

Preferred Advanced Degrees:

  • MBA

  • MSc

  • MPH

  • PharmD

  • PhD

  • Equivalent advanced degree in a relevant discipline


Experience

  • 6–8+ years of experience in:

    • Clinical Analytics

    • Trial Analytics

    • Clinical Operations

    • Management Consulting

    • Clinical Strategy

    • Pharmaceutical Research

Therapeutic Area Experience Preferred

  • Oncology

  • Neuroscience

  • Cell Therapy

  • Hematology

  • Immunology

  • Cardiovascular Disease


Technical Skills

  • Advanced Microsoft Excel

  • Power BI

  • R Programming

  • Python

  • Clinical Trial Analytics Platforms

  • Forecasting Models

  • Dashboard Development

  • Data Visualization


Core Competencies

Leadership

  • Team Management

  • Coaching & Mentoring

  • Stakeholder Management

Analytical Skills

  • Strategic Thinking

  • Data Interpretation

  • Forecasting

  • Problem Solving

Communication

  • Executive Presentation Skills

  • Cross-functional Collaboration

  • Consulting Mindset

Business Acumen

  • Clinical Trial Optimization

  • Cost Analysis

  • Resource Planning

  • Strategic Decision Making


Why This Role is Attractive

High Strategic Impact

Influence trial design, planning, and execution for global clinical studies.

Leadership Opportunity

Lead a global team while working directly with senior stakeholders.

Internal Consulting Exposure

Operate as a trusted advisor to study teams and business leaders.

Career Growth

Clear progression path into:

  • Associate Director

  • Director

  • Senior Director

  • Enterprise Strategy Leadership

Potential Total Compensation

  • Fixed Salary

  • Annual Performance Bonus (10–20%)

  • Long-Term Incentives (role dependent)

  • Health Insurance

  • Provident Fund (PF)

  • Learning & Development Programs

  • Hybrid Work Benefits

  • Employee Wellness Programs


Work Model

Hybrid (Site-by-Design)

  • Minimum 50% onsite presence required.

  • Remaining work can be performed remotely based on company policy.


Ideal Candidate Profile

A professional with 6–10 years of experience in clinical analytics, trial strategy, management consulting, or clinical operations, possessing strong leadership skills, expertise in forecasting and trial optimization, and the ability to influence global study decisions through advanced analytics and strategic insights.