PHARMAFull-time
Associate Director, TAIP Principal Analyst_Trial Analytics, Insights & Planning (TAIP)
By Admin · Data Science, Analytics & AI
HYDERABAD (IN)HYBRIDPOSTED: 9/4/2026
PHARMAFull-time
HIRING ORGANIZATIONBRISTOL MYERS SQUIBBPharmaceuticals
BR
ROLE DEFINITION & RESPONSIBILITIES
Position Summary
Mid-senior level position within BMS's Trial Analytics, Insights & Planning (TAIP) organization, an internal consulting team focused on accelerating clinical development through advanced analytics and strategic trial planning.
Own end-to-end analytics delivery for one or more global clinical trials and act as the key analytics partner embedded within study teams.
Lead a global project team of 3–5 Analysts and Senior Analysts, ensuring high-quality, coordinated, and timely delivery.
Translate clinical-trial needs into data-driven strategies covering feasibility, forecasting, optimization, performance tracking, and decision support.
Core Responsibilities
Own study-level analytics planning and delivery from protocol concept through trial execution.
Lead and coordinate a team of 3–5 Analysts/Senior Analysts in a global trial-delivery environment.
Translate study objectives into analytical workstreams including feasibility analysis, enrollment forecasting, site scoring, and performance dashboards.
Partner directly with clinical, feasibility, operations, and therapeutic-area leads to ensure analytical alignment and scientific rigor.
Contribute to cost analysis, including assessment of country-mix options and protocol-design trade-offs.
Lead study-optimization analytics covering patient burden, site burden, competitive trial landscape, and other relevant data sources.
Incorporate field-based/on-the-ground insights into feasibility assessments and site strategy.
Use advanced analytics tools and platforms to generate, structure, analyze, and communicate clinical-trial data.
Support planning and forecasting affecting clinical supplies, patient flow, and site-level requirements.
Ensure consistency and scalability of analytical tools, assumptions, methodologies, and outputs across trials and teams.
Identify risks, escalate issues, and develop data-driven opportunities to accelerate clinical-trial execution.
Provide data and insights to clinical supply teams to align clinical planning with supply-chain requirements.
Apply critical thinking to complex datasets, challenge assumptions, and generate strategic evidence-based recommendations.
Technical & Domain Expertise
Strong foundation in clinical-trial science and applied analytics.
Understanding of clinical protocol design and patient-population logic.
Experience developing/interpreting forecasting models, dashboards, operational metrics, feasibility analyses, and trial-performance analytics.
Exposure to recruitment strategies, social-media inputs, field intelligence, competitive trial information, cost analytics, and study optimization.
Experience with Excel, Power BI, R, and/or Python is advantageous.
Strong knowledge of at least one relevant therapeutic area: Oncology, Neuroscience, Cell Therapy, Hematology, Immunology, or Cardiovascular.
Leadership & Business Impact
Lead and develop a global team of Analysts and Senior Analysts.
Operate as an internal consultant to clinical-study leadership and influence trial strategy through analytics.
Manage multiple priorities and work effectively with cross-functional and global stakeholders.
Help design smarter, faster clinical trials and improve patient access to innovative therapies.
Qualifications
Preferred advanced degree such as MBA, MSc, MPH, PharmD, PhD, or equivalent relevant qualification.
Requires 6–8+ years of experience in clinical analytics, management consulting, or trial strategy.
Prior exposure to clinical-trial delivery processes and data-driven decision-making is required.
Proven cross-functional leadership and ability to manage multiple priorities.
Strong structured problem-solving and communication skills.
Comfortable operating in fast-paced, matrixed global environments.
Work Environment & BMS Offering
Hyderabad-based global role within BMS's TAIP organization.
BMS describes work models including site-essential, site-by-design, field-based, and remote-by-design; the assigned model depends on role responsibilities.
BMS highlights inclusion, wellbeing, flexibility, comprehensive benefits, professional development, and opportunities to work on meaningful clinical-development programs.
REQUIRED VERIFIED SKILLS
6–8+ years clinical analytics
Management consulting
Trial strategy
Clinical trial delivery
Clinical trial science
Applied analytics
Study-level analytics
Feasibility analysis
Enrollment forecasting
Site scoring
Performance dashboards
Forecasting models
Clinical trial optimization
Cost analysis
Country mix analysis
Protocol design analysis
Patient burden analysis
Site burden analysis
Clinical supply planning
Data-driven decision making
Structured problem solving
Cross-functional leadership
Global team collaboration
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
No salary range or specific monetary compensation is disclosed in the official posting. The role is an Associate Director-level position requiring 6–8+ years of experience, so compensation would normally reflect senior clinical analytics/consulting market positioning. Candidates should assess the complete BMS package, including fixed pay, potential variable compensation, benefits, wellbeing programs, flexibility, professional development, and long-term career progression. Do not assume a specific INR salary without an official offer or compensation disclosure.
ORGANIZATION CONTEXT & CULTURE
Bristol Myers Squibb is actively hiring for this position.
INDUSTRY: Pharmaceuticals
EXPECTED CAREER ROADMAP
The role offers a structured consulting-style career path with transparent expectations and an approximate 2–3 years per level. It provides direct experience in global clinical-trial strategy, advanced analytics, internal consulting, and team leadership. Successful performance can lead toward broader strategy leadership, enterprise-level consulting, senior analytics leadership, and other strategic positions across BMS. The role also develops transferable expertise in clinical development, data analytics, forecasting, trial optimization, stakeholder leadership, and clinical supply strategy, supporting long-term progression across pharmaceutical, biotechnology, healthcare analytics, and life-sciences consulting.
APPLICATION ADVISORY
Emphasize 6–8+ years of clinical analytics, trial strategy, management consulting, or clinical operations experience. Quantify ownership of clinical-trial analytics, feasibility, enrollment forecasting, site selection/scoring, dashboards, optimization, cost analysis, or supply forecasting. Highlight leadership of analysts or cross-functional global teams. Demonstrate therapeutic-area expertise, particularly Oncology, Neuroscience, Cell Therapy, Hematology, Immunology, or Cardiovascular. Showcase Excel, Power BI, R, and Python where applicable. Prepare examples showing how analytics changed a trial decision, improved enrollment, reduced site/patient burden, optimized country mix, identified risks, or supported clinical supply planning. Be ready for case-style questions involving clinical-trial feasibility, forecasting, site strategy, data interpretation, stakeholder management, and structured problem solving. This is not a fresher role; candidates should clearly demonstrate senior-level ownership and leadership.
RECOMMENDED TRAINING
1/5
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