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

Bristol-Myers Squibb

Healthcare Jobs

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

full-timePosted: Nov 4, 2025

Job Description

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 Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Education: Preferred advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field 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 Strong scientific and analytical thinking applied in a clinical trial context Ability to link insights to strategy and influence TA-level decision-making Excellent leadership, communication, and stakeholder management skills Familiarity with forecasting models, dashboards, and feasibility tools is a plus

Key Responsibilities

  • Lead analytics strategy and delivery across a portfolio of trials within assigned Therapeutic Area (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 to shape trial strategy and portfolio-level planning through data-driven insights
  • Ensure cross-trial consistency and innovation in forecasting, feasibility modeling, 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
  • Apply critical thinking to analyze complex data, challenge assumptions, and generate strategic, evidence-based recommendations

Required Qualifications

  • Advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field
  • + years in management consulting, trial analytics, or clinical strategy
  • Deep experience in one or more therapeutic areas: Oncology, Neuroscience, Cell Therapy, Hematology, Immunology, or Cardiovascular

Preferred Qualifications

  • Familiarity with forecasting models, dashboards, and feasibility tools

Skills Required

  • Proven ability to lead teams, engage with senior stakeholders, and operate effectively across global functions
  • Strong scientific and analytical thinking applied in a clinical trial context
  • Ability to link insights to strategy and influence TA-level decision-making
  • Excellent leadership, communication, and stakeholder management skills

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Locations

  • Princeton NJ, United States

Salary

Estimated Salary Rangemedium confidence

150,000 - 250,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Proven ability to lead teams, engage with senior stakeholders, and operate effectively across global functionsintermediate
  • Strong scientific and analytical thinking applied in a clinical trial contextintermediate
  • Ability to link insights to strategy and influence TA-level decision-makingintermediate
  • Excellent leadership, communication, and stakeholder management skillsintermediate

Required Qualifications

  • Advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field (experience)
  • + years in management consulting, trial analytics, or clinical strategy (experience)
  • Deep experience in one or more therapeutic areas: Oncology, Neuroscience, Cell Therapy, Hematology, Immunology, or Cardiovascular (experience)

Preferred Qualifications

  • Familiarity with forecasting models, dashboards, and feasibility tools (experience)

Responsibilities

  • Lead analytics strategy and delivery across a portfolio of trials within assigned Therapeutic Area (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 to shape trial strategy and portfolio-level planning through data-driven insights
  • Ensure cross-trial consistency and innovation in forecasting, feasibility modeling, 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
  • Apply critical thinking to analyze complex data, challenge assumptions, and generate strategic, evidence-based recommendations

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

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Bristol-Myers Squibb logo

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

Bristol-Myers Squibb

Healthcare Jobs

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

full-timePosted: Nov 4, 2025

Job Description

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 Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Education: Preferred advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field 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 Strong scientific and analytical thinking applied in a clinical trial context Ability to link insights to strategy and influence TA-level decision-making Excellent leadership, communication, and stakeholder management skills Familiarity with forecasting models, dashboards, and feasibility tools is a plus

Key Responsibilities

  • Lead analytics strategy and delivery across a portfolio of trials within assigned Therapeutic Area (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 to shape trial strategy and portfolio-level planning through data-driven insights
  • Ensure cross-trial consistency and innovation in forecasting, feasibility modeling, 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
  • Apply critical thinking to analyze complex data, challenge assumptions, and generate strategic, evidence-based recommendations

Required Qualifications

  • Advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field
  • + years in management consulting, trial analytics, or clinical strategy
  • Deep experience in one or more therapeutic areas: Oncology, Neuroscience, Cell Therapy, Hematology, Immunology, or Cardiovascular

Preferred Qualifications

  • Familiarity with forecasting models, dashboards, and feasibility tools

Skills Required

  • Proven ability to lead teams, engage with senior stakeholders, and operate effectively across global functions
  • Strong scientific and analytical thinking applied in a clinical trial context
  • Ability to link insights to strategy and influence TA-level decision-making
  • Excellent leadership, communication, and stakeholder management skills

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Locations

  • Princeton NJ, United States

Salary

Estimated Salary Rangemedium confidence

150,000 - 250,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Proven ability to lead teams, engage with senior stakeholders, and operate effectively across global functionsintermediate
  • Strong scientific and analytical thinking applied in a clinical trial contextintermediate
  • Ability to link insights to strategy and influence TA-level decision-makingintermediate
  • Excellent leadership, communication, and stakeholder management skillsintermediate

Required Qualifications

  • Advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field (experience)
  • + years in management consulting, trial analytics, or clinical strategy (experience)
  • Deep experience in one or more therapeutic areas: Oncology, Neuroscience, Cell Therapy, Hematology, Immunology, or Cardiovascular (experience)

Preferred Qualifications

  • Familiarity with forecasting models, dashboards, and feasibility tools (experience)

Responsibilities

  • Lead analytics strategy and delivery across a portfolio of trials within assigned Therapeutic Area (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 to shape trial strategy and portfolio-level planning through data-driven insights
  • Ensure cross-trial consistency and innovation in forecasting, feasibility modeling, 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
  • Apply critical thinking to analyze complex data, challenge assumptions, and generate strategic, evidence-based recommendations

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

Target Your Resume for "Director, TAIP TA Lead – Trial Analytics, Insights & Planning (TAIP)" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Director, TAIP TA Lead – Trial Analytics, Insights & Planning (TAIP). Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Director, TAIP TA Lead – Trial Analytics, Insights & Planning (TAIP)" , Bristol-Myers Squibb

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

Answer 10 quick questions to check your fit for Director, TAIP TA Lead – Trial Analytics, Insights & Planning (TAIP) @ Bristol-Myers Squibb.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.