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Associate Director, TAIP Principal Analyst - Trial Analytics, Insights & Planning; TAIP

Job in Princeton, Mercer County, New Jersey, 08543, USA
Listing for: Bristol-Myers Squibb Co
Full Time position
Listed on 2026-01-07
Job specializations:
  • IT/Tech
    Data Science Manager, Data Analyst, Business Systems/ Tech Analyst
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below
Position: Associate Director, TAIP Principal Analyst - Trial Analytics, Insights & Planning (TAIP)

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

Join to apply for the Associate Director, TAIP Principal Analyst - Trial Analytics, Insights & Planning (TAIP) role at Bristol Myers Squibb
.

Working with Us

Challenging. Meaningful. Life‑changing. Those aren't words typically associated with a job, but working at Bristol Myers Squibb is anything but ordinary. Here, uniquely interesting work happens every day, in every department— from optimizing a production line to breakthroughs in cell therapy. You’ll have the chance to grow and thrive through opportunities uncommon at scale, alongside high‑achieving teams. Take your career farther than you imagined.

Bristol Myers Squibb recognizes the importance of balance and flexibility. We offer competitive benefits, services, and programs that allow employees to pursue their goals, both at work and in personal life. Read more:

Position Summary

The TAIP Principal Analyst is a mid‑senior level role within Bristol Myers Squibb's Trial Analytics, Insights, and Planning (TAIP) organization—an internal consulting team focused on accelerating clinical development through advanced analytics and strategic trial planning. In this role you will lead end‑to‑end analytics delivery for one or more clinical trials, managing a global project team of 3–5 analysts and senior analysts.

Embedded within the study team, you will serve as the key analytics partner, translating trial needs into data‑driven strategies, coordinating feasibility, forecasting, and performance tracking, and driving informed decision‑making throughout execution.

With a strong foundation in both clinical trial science and applied analytics, you will develop forecasting models, dashboards, and operational metrics. You will also contribute to integrating insights from recruitment strategies, social media, and field‑based inputs while supporting study design decisions informed by cost and optimization analytics. This is an ideal opportunity for professionals with backgrounds in consulting, clinical operations, or trial analytics who are ready to take ownership of delivery and help shape the success of global studies.

Key Responsibilities
  • Own study‑level analytics planning and delivery from protocol concept through execution.
  • Lead a project team of 3–5 analysts and senior analysts, ensuring coordinated, high‑quality, and timely execution of deliverables.
  • Translate study objectives into analytical work streams, including feasibility, enrollment forecasting, site scoring, and performance dashboards.
  • Engage directly with cross‑functional study team members (clinical, feasibility, ops, TA leads) to ensure alignment and scientific rigor in all analytics.
  • Contribute to cost analysis efforts, including evaluating country mix and protocol design trade‑offs.
  • Lead study optimization analytics, including assessment of patient and site burden, competitive trial landscape, and other key data sources.
  • Coordinate with field‑based teams to incorporate on‑ground insights into feasibility and site strategy.
  • Utilize advanced analytics tools and platforms to generate, structure, and communicate trial data.
  • Support planning and forecasting activities with implications for clinical supply, patient flow, and site‑level requirements.
  • Ensure consistency and scalability in tools, assumptions, and outputs across trials and teams.
  • Escalate risks and identify opportunities to accelerate trial execution using data‑driven insights.
  • Provide relevant data and insights to support clinical supply team, ensuring alignment between clinical planning and supply chain requirements.
  • Apply critical thinking to analyze complex data, challenge assumptions, and generate strategic, evidence‑based recommendations.
Qualifications & Experience
  • Education: Preferred advanced degree (MBA, MSc, MPH, Pharm

    D, PhD, or equivalent) in a relevant field.
  • Experience:
    • 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.
    • Strong therapeutic area knowledge in one or more of:
      Oncology, Neuroscience, Cell Therapy, Hematology,…
Position Requirements
10+ Years work experience
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