Sr. Director, TAIP TA Lead – Trial Analytics, Insights, and Planning (TAIP)
Bristol-Myers Squibb
Sr. Director, TAIP TA Lead – Trial Analytics, Insights, and Planning (TAIP)
Job Description
Manage a team of direct reports, including performance management, career development, and day-to-day support Lead the analytics strategy and execution across a global 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 Serve as a strategic advisor to TA leadership, shaping trial strategy, feasibility, 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 Contribute to the enterprise evolution of TAIP, defining best practices, mentoring talent, and elevating analytics standards 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 10+ 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 Strategic and analytical thinker with the ability to translate data-driven insights into enterprise-level decisions Excellent leadership, communication, and stakeholder management skills Familiarity with forecasting models, dashboards, and feasibility tools is a plus
Key Responsibilities
- Manage a team of direct reports, including performance management, career development, and day-to-day support
- Lead the analytics strategy and execution across a global 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
- Serve as a strategic advisor to TA leadership, shaping trial strategy, feasibility, 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
- Contribute to the enterprise evolution of TAIP, defining best practices, mentoring talent, and elevating analytics standards 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 preferred
- 0+ years of experience in management consulting, trial analytics, or clinical strategy required
- 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
- Strategic and analytical thinker with the ability to translate data-driven insights into enterprise-level decisions
- 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
250,000 - 350,000 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
- Strategic and analytical thinker with the ability to translate data-driven insights into enterprise-level decisionsintermediate
- Excellent leadership, communication, and stakeholder management skillsintermediate
Required Qualifications
- Advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field preferred (experience)
- 0+ years of experience in management consulting, trial analytics, or clinical strategy required (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
- Manage a team of direct reports, including performance management, career development, and day-to-day support
- Lead the analytics strategy and execution across a global 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
- Serve as a strategic advisor to TA leadership, shaping trial strategy, feasibility, 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
- Contribute to the enterprise evolution of TAIP, defining best practices, mentoring talent, and elevating analytics standards 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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Sr. Director, TAIP TA Lead – Trial Analytics, Insights, and Planning (TAIP)
Bristol-Myers Squibb
Sr. Director, TAIP TA Lead – Trial Analytics, Insights, and Planning (TAIP)
Job Description
Manage a team of direct reports, including performance management, career development, and day-to-day support Lead the analytics strategy and execution across a global 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 Serve as a strategic advisor to TA leadership, shaping trial strategy, feasibility, 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 Contribute to the enterprise evolution of TAIP, defining best practices, mentoring talent, and elevating analytics standards 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 10+ 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 Strategic and analytical thinker with the ability to translate data-driven insights into enterprise-level decisions Excellent leadership, communication, and stakeholder management skills Familiarity with forecasting models, dashboards, and feasibility tools is a plus
Key Responsibilities
- Manage a team of direct reports, including performance management, career development, and day-to-day support
- Lead the analytics strategy and execution across a global 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
- Serve as a strategic advisor to TA leadership, shaping trial strategy, feasibility, 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
- Contribute to the enterprise evolution of TAIP, defining best practices, mentoring talent, and elevating analytics standards 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 preferred
- 0+ years of experience in management consulting, trial analytics, or clinical strategy required
- 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
- Strategic and analytical thinker with the ability to translate data-driven insights into enterprise-level decisions
- 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
250,000 - 350,000 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
- Strategic and analytical thinker with the ability to translate data-driven insights into enterprise-level decisionsintermediate
- Excellent leadership, communication, and stakeholder management skillsintermediate
Required Qualifications
- Advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field preferred (experience)
- 0+ years of experience in management consulting, trial analytics, or clinical strategy required (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
- Manage a team of direct reports, including performance management, career development, and day-to-day support
- Lead the analytics strategy and execution across a global 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
- Serve as a strategic advisor to TA leadership, shaping trial strategy, feasibility, 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
- Contribute to the enterprise evolution of TAIP, defining best practices, mentoring talent, and elevating analytics standards 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
Tags & Categories
Answer 10 quick questions to check your fit for Sr. Director, TAIP TA Lead – Trial Analytics, Insights, and Planning (TAIP) @ Bristol-Myers Squibb.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs