Sr. Director, TA Lead - Trial Analytics, Insights, and Planning (TAIP)

Bristol Myers Squibb EU Policy; Princeton (NJ); On-site; USD 234,000 - 317,000; Full time

Benefits offered by this job

Health coverage

Wellbeing programs

Financial well-being: 401(k)

Job summary

Bristol Myers Squibb in Princeton, NJ seeks a Sr Director, TA Lead to steer analytics for the Oncology portfolio. You will own end-to-end analytics strategy, oversee feasibility, enrollment forecasting, and cross-functional delivery to improve trial timelines and quality.

You will lead a global team, partner with TA medical, clinical, and operations leadership, and translate data-driven insights into practical strategies that advance the enterprise.

Qualifications

• Advanced degree in a relevant field such as Biology, Medicine, Data Science, Computer Science or related field.
• 10+ years in management consulting, trial analytics, or clinical strategy.
• Deep experience in Oncology or related fields.

Responsibilities

• Lead analytics strategy for a global portfolio of oncology trials.
• Manage a team of analysts; oversee performance and development.
• Provide day-to-day coaching and direction to analytics leads.
• Partner with TA leadership to shape trial strategy and feasibility.
• Ensure cross-trial consistency in forecasting and dashboards.

Skills

Strategic thinking

Analytical skills

Leadership

Stakeholder management

Forecasting models

Dashboards

Communication

Education

Advanced degree in a relevant field (MBA, MSc, MPH, PharmD, PhD)

Tools

Forecasting models

Dashboards

Site feasibility tools

Job description

Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

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 the Oncology therapeutic area (TA), you will be accountable for the end-to-end analytics strategy and execution across a global portfolio of clinical trials within that TA—supporting trial-level planning, overseeing delivery performance, and leading a team of analytics professionals across multiple levels and geographies. This role will have direct reports across different levels of seniority, and the incumbent will provide day-to-day direction, coaching, and performance management.

You will serve as a strategic thought partner to TA medical, clinical, and operational leadership, influencing decisions that directly impact trial timelines, cost, and quality. You will be responsible for providing 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 serve as a trusted partner to TA medical, clinical, and operational leadership.

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

Key Responsibilities

• Manage a team of analysts, including accountability for performance management, career development, and day-to-day support
• Lead the analytics strategy and execution across a global portfolio of oncology trials
• 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

Qualifications & Experience

Education:

• Advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field preferred such as Biology, Medicine, Data Science, Computer Science, Clinical Research, etc.

Experience

• 10+ years in management consulting, trial analytics, or clinical strategy is required
• Direct experience with clinical trial feasibility, enrollment forecasting, and operational analytics
• Deep experience in Oncology or related fields
• Proven ability to lead teams, engage with senior stakeholders, and operate effectively across global functions
• Demonstrated experience delivering under tight timelines and comfortable operating in a fast-paced environment

Skills

• Strategic and analytical thinker with the ability to translate data-driven insights into enterprise-level decisions
• Excellent leadership, communication, and stakeholder management skills
• Direct experience with building forecasting models, dashboards, and site feasibility tools is a plus

Why Join This Team?

• Drive strategic clinical impact: Leverage data, analytics, and scientific expertise to inform smarter, faster development decisions that bring therapies to patients sooner
• Shape the future of analytics leadership: As member of the TAIP leadership team, you will help define the future of trial analytics at BMS—setting standards, mentoring talent, and influencing the evolution of data-driven trial planning across the enterprise
• Pathway to enterprise leadership: This role is a launchpad for broader strategic and leadership opportunities across BMS
• Collaborate globally, drive locally: Operate as part of a distributed team while anchoring analytics leadership within your therapeutic area

Compensation Overview

Cambridge Crossing: $261,840 - $317,292

Princeton - NJ - US: $233,780 - $283,291

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.

Benefits

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

• Health Coverage: Medical, pharmacy, dental and vision care.
• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support and survivor support.

Work-life Benefits Include

Paid Time Off

• US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
• Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

• Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Responsibilities

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People With Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [e-mail]. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1605158 : Sr. Director, TA Lead - Trial Analytics, Insights, and Planning (TAIP)