Director, TAIP TA Lead – Trial Analytics, Insights & Planning (TAIP)

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Position Summary

The TAIP TA Lead is a senior leadership role reporting directly to the Head of the TAIP unit within Bristol Myers Squibb’s Trial Analytics, Insights, and Planning (TAIP) organization—an internal consulting team that drives clinical development excellence through data-driven insights, feasibility modelling, and strategic trial planning.

As the analytics lead for a therapeutic area (TA), you will be responsible for the full portfolio of trials within that TA—owning analytics strategy, resource planning, and delivery oversight. You’ll provide strategic direction, hands-on support, and quality control across studies while coaching study-level analytics leads and coordinating cross-trial priorities. You will act as a sounding board and escalation point for delivery-focused team members and a trusted partner to TA medical, clinical, and operational leadership.

This role requires a strong foundation in both clinical trial science and applied analytics, along with the ability to translate insights into strategies that directly impact trial timelines and delivery outcomes. You will also play a key role in evolving TAIP capabilities, ensuring consistency across methods, fostering innovation, and driving measurable business impact.

We are hiring TAIP TA Leads with experience in one or more of the following areas: Oncology, Neuroscience, Cell Therapy, Hematology, Immunology, or Cardiovascular.

Key Responsibilities

• Lead analytics strategy and delivery across a portfolio of trials within your assigned TA

• Guide, support, and review work across study-level analytics leads, acting as both coach and strategic sounding board

• Track delivery progress across trials, escalating risks and ensuring alignment with trial milestones and enterprise priorities

• Partner with clinical, medical, and operational leadership, shaping trial strategy and portfolio-level planning through data-driven insights

• Ensure cross-trial consistency and innovation in forecasting, feasibility modelling, performance dashboards, and protocol analytics

• Promote global collaboration, coordinating across teams to ensure effective, scalable delivery

• Lead discussions on cost implications of country mix and study design decisions at the portfolio level

• Promote study optimization analytics across trials, including evaluation of patient and site burden and competitive landscape data

• Coordinate field-based insights into TA-wide feasibility and site prioritization approaches

• Champion use of platforms, tools, and data infrastructure that support delivery excellence

• Integrate analytics with clinical supply planning where relevant to ensure delivery-readiness

• Influence the evolution of TAIP capabilities, helping define best practices and raise the bar on analytics excellence across trials

• Applies critical thinking to analyze complex data, challenge assumptions, and generate strategic, evidence-based recommendations

Qualifications & Experience

• Education: Preferred advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field

• Experience:

  • 8+ years in management consulting, trial analytics, or clinical strategy is required

  • Deep experience in one or more therapeutic areas: Oncology, Neuroscience, Cell Therapy, Hematology, Immunology, or Cardiovascular

  • Proven ability to lead teams, engage with senior stakeholders, and operate effectively across global functions

• Skills:

  • Strong scientific and analytical