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Bristol-Myers Squibb logo

Executive Director, Medical Evidence Generation Cell Therapy, Global Medical Affairs

Bristol-Myers Squibb

Executive Director, Medical Evidence Generation Cell Therapy, Global Medical Affairs

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 24, 2025

Number of Vacancies: 1

Job Description

Strategic Planning: Develop the 3-year strategic MEG plan for Cell Therapy and provide oversight of this portfolio of studies and thought partnership on trade-offs across studies to the worldwide TA (WWTA) and HEOR partners. Integrated Evidence Planning: Drive the development and maintenance of the IEPs for the Cell Therapy assets/indications, that align with unmet medical needs and business priorities, in partnership with WWTA teams, HEOR, GDD and other key internal stakeholders. Portfolio Leadership: Overall end to end responsibility for the medical oversight of Cell Therapy MEG book of work (Medical Affairs sponsored studies, clinical research collaborations and investigator-sponsored studies) ensuring they are on strategy and executed with rigor and on time. Collaboration/Matrix Leadership. Serve as a matrix partner with CT Leadership Team, Global Medical and International Medical teams. Facilitate Medical governance through the TAG forum and support MEG leads in executing EGWG meetings. Innovation and Data Driven Decision Making: Foster an innovative culture and lead initiatives to increase innovative approaches to evidence generation and lead with business savviness to leverage data analytics to define value drivers that will drive data-driven decisions. Portfolio Execution: Provide scientific oversight and clinical decision-making responsibility for studies within remit, inclusive of the conception, writing and monitoring of BMS-sponsored, medically-led research studies and ensures their timely accrual and completion. Ensure fiscal responsibility by maintaining a balanced budget for MEG Book of Work (BOW). Chair the Review Committees or contribute during the approval process for final protocols, amendments, and budgets for studies under remit. Serve as the subject matter expert on the current book of work for studies under remit and give updates to senior leadership/key stakeholders across the organization. Skillful Leadership: Lead and mentor a team of MEG Leads, Clinical Scientists, Clinical Trial Physicians and project managers to ensure strategic and rigorous execution of all scientific aspects associated with evidence generation activities. External Engagement: Serve as a trusted expert in meetings with investigators, external stakeholders and cross-functional internal teams involved in studies under remit to discuss scientific rational and expected impact, challenges associated with execution, budget concerns, and/or data readouts. 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. Supporting People with Disabilities Advanced scientific degree (e.g. Pharm.D., MD, PhD) with 10+ years of experience; 5+ years clinical trial expertise with a mix of development/clinical and medical with an emphasis on conduct / execution of trials Formal specialization in areas associated with the current cell therapy portfolio and/or professional experience with assets in this space is preferred. Cross-Functional Alignment & Influence: Proven ability to align across diverse teams and influence stakeholders toward shared success. Outcome-Driven Execution: Demonstrated capability to drive initiatives beyond effectiveness, ensuring measurable impact and results. Matrix Team Leadership: Experience leading high-performing matrixed teams to deliver strategic outcomes and organizational impact. People Management Excellence: Strong track record of managing and developing talent with a focus on performance, engagement, and growth. Entrepreneurial Mindset: Ability to anticipate market dynamics and identify opportunities to accelerate pipeline development. The successful candidate should have strong analytical skills, strong scientific data and evidence interpretation + contextualization and ability to work effectively with cross functional teams including clinical, commercialization, regulatory, HEOR and Access. Entrepreneurial thinking, anticipates needs, assesses and manages business and organizational risks. Highly organized and motivated and possess excellent people management, interpersonal, and strong communication skills. HQ based position with international/domestic travel requirement approximately 20%

About the Role/Company

  • The company focuses on Cell Therapy and Global Medical Affairs
  • The role involves working with various internal teams such as WWTA, HEOR, GDD, and others
  • The company values innovation, data-driven decision making, and cross-functional collaboration

Key Responsibilities

  • Develop the 3-year strategic MEG plan for Cell Therapy
  • Provide oversight of the portfolio of studies and thought partnership on trade-offs across studies to the worldwide TA (WWTA) and HEOR partners
  • Drive the development and maintenance of the IEPs for the Cell Therapy assets/indications
  • Ensure alignment with unmet medical needs and business priorities in partnership with WWTA teams, HEOR, GDD and other key internal stakeholders
  • Overall end to end responsibility for the medical oversight of Cell Therapy MEG book of work
  • Ensure studies are on strategy and executed with rigor and on time
  • Serve as a matrix partner with CT Leadership Team, Global Medical and International Medical teams
  • Facilitate Medical governance through the TAG forum and support MEG leads in executing EGWG meetings
  • Foster an innovative culture and lead initiatives to increase innovative approaches to evidence generation
  • Leverage data analytics to define value drivers that will drive data-driven decisions
  • Provide scientific oversight and clinical decision-making responsibility for studies within remit
  • Ensure fiscal responsibility by maintaining a balanced budget for MEG Book of Work (BOW)
  • Chair the Review Committees or contribute during the approval process for final protocols, amendments, and budgets for studies under remit
  • Serve as the subject matter expert on the current book of work for studies under remit
  • Give updates to senior leadership/key stakeholders across the organization
  • Lead and mentor a team of MEG Leads, Clinical Scientists, Clinical Trial Physicians and project managers
  • Ensure strategic and rigorous execution of all scientific aspects associated with evidence generation activities
  • Serve as a trusted expert in meetings with investigators, external stakeholders and cross-functional internal teams
  • Discuss scientific rational and expected impact, challenges associated with execution, budget concerns, and/or data readouts

Required Qualifications

  • Advanced scientific degree (e.g., Pharm.D., MD, PhD)
  • 0+ years of experience
  • + years clinical trial expertise with a mix of development/clinical and medical with an emphasis on conduct/execution of trials

Preferred Qualifications

  • Formal specialization in areas associated with the current cell therapy portfolio
  • Professional experience with assets in cell therapy space

Skills Required

  • Strong analytical skills
  • Strong scientific data and evidence interpretation and contextualization
  • Ability to work effectively with cross-functional teams including clinical, commercialization, regulatory, HEOR and Access
  • Entrepreneurial thinking
  • Ability to anticipate needs, assess and manage business and organizational risks
  • Highly organized and motivated
  • Excellent people management skills
  • Excellent interpersonal skills
  • Strong communication skills
  • Proven ability to align across diverse teams and influence stakeholders toward shared success
  • Demonstrated capability to drive initiatives beyond effectiveness, ensuring measurable impact and results
  • Experience leading high-performing matrixed teams to deliver strategic outcomes and organizational impact
  • Strong track record of managing and developing talent with a focus on performance, engagement, and growth
  • Ability to anticipate market dynamics and identify opportunities to accelerate pipeline development

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
  • Programs supporting people with disabilities

Additional Requirements

  • HQ based position
  • International/domestic travel requirement approximately 20%

Locations

  • Princeton Pike, NJ
  • Madison Giralda NJ, United States
  • Boudry, Switzerland
  • Uxbridge, GB
  • Princeton NJ, United States

Salary

Salary not disclosed

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

  • Strong analytical skillsintermediate
  • Strong scientific data and evidence interpretation and contextualizationintermediate
  • Ability to work effectively with cross-functional teams including clinical, commercialization, regulatory, HEOR and Accessintermediate
  • Entrepreneurial thinkingintermediate
  • Ability to anticipate needs, assess and manage business and organizational risksintermediate
  • Highly organized and motivatedintermediate
  • Excellent people management skillsintermediate
  • Excellent interpersonal skillsintermediate
  • Strong communication skillsintermediate
  • Proven ability to align across diverse teams and influence stakeholders toward shared successintermediate
  • Demonstrated capability to drive initiatives beyond effectiveness, ensuring measurable impact and resultsintermediate
  • Experience leading high-performing matrixed teams to deliver strategic outcomes and organizational impactintermediate
  • Strong track record of managing and developing talent with a focus on performance, engagement, and growthintermediate
  • Ability to anticipate market dynamics and identify opportunities to accelerate pipeline developmentintermediate

Required Qualifications

  • Advanced scientific degree (e.g., Pharm.D., MD, PhD) (experience)
  • 0+ years of experience (experience)
  • + years clinical trial expertise with a mix of development/clinical and medical with an emphasis on conduct/execution of trials (experience)

Preferred Qualifications

  • Formal specialization in areas associated with the current cell therapy portfolio (experience)
  • Professional experience with assets in cell therapy space (experience)

Responsibilities

  • Develop the 3-year strategic MEG plan for Cell Therapy
  • Provide oversight of the portfolio of studies and thought partnership on trade-offs across studies to the worldwide TA (WWTA) and HEOR partners
  • Drive the development and maintenance of the IEPs for the Cell Therapy assets/indications
  • Ensure alignment with unmet medical needs and business priorities in partnership with WWTA teams, HEOR, GDD and other key internal stakeholders
  • Overall end to end responsibility for the medical oversight of Cell Therapy MEG book of work
  • Ensure studies are on strategy and executed with rigor and on time
  • Serve as a matrix partner with CT Leadership Team, Global Medical and International Medical teams
  • Facilitate Medical governance through the TAG forum and support MEG leads in executing EGWG meetings
  • Foster an innovative culture and lead initiatives to increase innovative approaches to evidence generation
  • Leverage data analytics to define value drivers that will drive data-driven decisions
  • Provide scientific oversight and clinical decision-making responsibility for studies within remit
  • Ensure fiscal responsibility by maintaining a balanced budget for MEG Book of Work (BOW)
  • Chair the Review Committees or contribute during the approval process for final protocols, amendments, and budgets for studies under remit
  • Serve as the subject matter expert on the current book of work for studies under remit
  • Give updates to senior leadership/key stakeholders across the organization
  • Lead and mentor a team of MEG Leads, Clinical Scientists, Clinical Trial Physicians and project managers
  • Ensure strategic and rigorous execution of all scientific aspects associated with evidence generation activities
  • Serve as a trusted expert in meetings with investigators, external stakeholders and cross-functional internal teams
  • Discuss scientific rational and expected impact, challenges associated with execution, budget concerns, and/or data readouts

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
  • general: Programs supporting people with disabilities

Travel Requirements

0%

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Bristol-Myers Squibb logo

Executive Director, Medical Evidence Generation Cell Therapy, Global Medical Affairs

Bristol-Myers Squibb

Executive Director, Medical Evidence Generation Cell Therapy, Global Medical Affairs

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 24, 2025

Number of Vacancies: 1

Job Description

Strategic Planning: Develop the 3-year strategic MEG plan for Cell Therapy and provide oversight of this portfolio of studies and thought partnership on trade-offs across studies to the worldwide TA (WWTA) and HEOR partners. Integrated Evidence Planning: Drive the development and maintenance of the IEPs for the Cell Therapy assets/indications, that align with unmet medical needs and business priorities, in partnership with WWTA teams, HEOR, GDD and other key internal stakeholders. Portfolio Leadership: Overall end to end responsibility for the medical oversight of Cell Therapy MEG book of work (Medical Affairs sponsored studies, clinical research collaborations and investigator-sponsored studies) ensuring they are on strategy and executed with rigor and on time. Collaboration/Matrix Leadership. Serve as a matrix partner with CT Leadership Team, Global Medical and International Medical teams. Facilitate Medical governance through the TAG forum and support MEG leads in executing EGWG meetings. Innovation and Data Driven Decision Making: Foster an innovative culture and lead initiatives to increase innovative approaches to evidence generation and lead with business savviness to leverage data analytics to define value drivers that will drive data-driven decisions. Portfolio Execution: Provide scientific oversight and clinical decision-making responsibility for studies within remit, inclusive of the conception, writing and monitoring of BMS-sponsored, medically-led research studies and ensures their timely accrual and completion. Ensure fiscal responsibility by maintaining a balanced budget for MEG Book of Work (BOW). Chair the Review Committees or contribute during the approval process for final protocols, amendments, and budgets for studies under remit. Serve as the subject matter expert on the current book of work for studies under remit and give updates to senior leadership/key stakeholders across the organization. Skillful Leadership: Lead and mentor a team of MEG Leads, Clinical Scientists, Clinical Trial Physicians and project managers to ensure strategic and rigorous execution of all scientific aspects associated with evidence generation activities. External Engagement: Serve as a trusted expert in meetings with investigators, external stakeholders and cross-functional internal teams involved in studies under remit to discuss scientific rational and expected impact, challenges associated with execution, budget concerns, and/or data readouts. 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. Supporting People with Disabilities Advanced scientific degree (e.g. Pharm.D., MD, PhD) with 10+ years of experience; 5+ years clinical trial expertise with a mix of development/clinical and medical with an emphasis on conduct / execution of trials Formal specialization in areas associated with the current cell therapy portfolio and/or professional experience with assets in this space is preferred. Cross-Functional Alignment & Influence: Proven ability to align across diverse teams and influence stakeholders toward shared success. Outcome-Driven Execution: Demonstrated capability to drive initiatives beyond effectiveness, ensuring measurable impact and results. Matrix Team Leadership: Experience leading high-performing matrixed teams to deliver strategic outcomes and organizational impact. People Management Excellence: Strong track record of managing and developing talent with a focus on performance, engagement, and growth. Entrepreneurial Mindset: Ability to anticipate market dynamics and identify opportunities to accelerate pipeline development. The successful candidate should have strong analytical skills, strong scientific data and evidence interpretation + contextualization and ability to work effectively with cross functional teams including clinical, commercialization, regulatory, HEOR and Access. Entrepreneurial thinking, anticipates needs, assesses and manages business and organizational risks. Highly organized and motivated and possess excellent people management, interpersonal, and strong communication skills. HQ based position with international/domestic travel requirement approximately 20%

About the Role/Company

  • The company focuses on Cell Therapy and Global Medical Affairs
  • The role involves working with various internal teams such as WWTA, HEOR, GDD, and others
  • The company values innovation, data-driven decision making, and cross-functional collaboration

Key Responsibilities

  • Develop the 3-year strategic MEG plan for Cell Therapy
  • Provide oversight of the portfolio of studies and thought partnership on trade-offs across studies to the worldwide TA (WWTA) and HEOR partners
  • Drive the development and maintenance of the IEPs for the Cell Therapy assets/indications
  • Ensure alignment with unmet medical needs and business priorities in partnership with WWTA teams, HEOR, GDD and other key internal stakeholders
  • Overall end to end responsibility for the medical oversight of Cell Therapy MEG book of work
  • Ensure studies are on strategy and executed with rigor and on time
  • Serve as a matrix partner with CT Leadership Team, Global Medical and International Medical teams
  • Facilitate Medical governance through the TAG forum and support MEG leads in executing EGWG meetings
  • Foster an innovative culture and lead initiatives to increase innovative approaches to evidence generation
  • Leverage data analytics to define value drivers that will drive data-driven decisions
  • Provide scientific oversight and clinical decision-making responsibility for studies within remit
  • Ensure fiscal responsibility by maintaining a balanced budget for MEG Book of Work (BOW)
  • Chair the Review Committees or contribute during the approval process for final protocols, amendments, and budgets for studies under remit
  • Serve as the subject matter expert on the current book of work for studies under remit
  • Give updates to senior leadership/key stakeholders across the organization
  • Lead and mentor a team of MEG Leads, Clinical Scientists, Clinical Trial Physicians and project managers
  • Ensure strategic and rigorous execution of all scientific aspects associated with evidence generation activities
  • Serve as a trusted expert in meetings with investigators, external stakeholders and cross-functional internal teams
  • Discuss scientific rational and expected impact, challenges associated with execution, budget concerns, and/or data readouts

Required Qualifications

  • Advanced scientific degree (e.g., Pharm.D., MD, PhD)
  • 0+ years of experience
  • + years clinical trial expertise with a mix of development/clinical and medical with an emphasis on conduct/execution of trials

Preferred Qualifications

  • Formal specialization in areas associated with the current cell therapy portfolio
  • Professional experience with assets in cell therapy space

Skills Required

  • Strong analytical skills
  • Strong scientific data and evidence interpretation and contextualization
  • Ability to work effectively with cross-functional teams including clinical, commercialization, regulatory, HEOR and Access
  • Entrepreneurial thinking
  • Ability to anticipate needs, assess and manage business and organizational risks
  • Highly organized and motivated
  • Excellent people management skills
  • Excellent interpersonal skills
  • Strong communication skills
  • Proven ability to align across diverse teams and influence stakeholders toward shared success
  • Demonstrated capability to drive initiatives beyond effectiveness, ensuring measurable impact and results
  • Experience leading high-performing matrixed teams to deliver strategic outcomes and organizational impact
  • Strong track record of managing and developing talent with a focus on performance, engagement, and growth
  • Ability to anticipate market dynamics and identify opportunities to accelerate pipeline development

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
  • Programs supporting people with disabilities

Additional Requirements

  • HQ based position
  • International/domestic travel requirement approximately 20%

Locations

  • Princeton Pike, NJ
  • Madison Giralda NJ, United States
  • Boudry, Switzerland
  • Uxbridge, GB
  • Princeton NJ, United States

Salary

Salary not disclosed

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

  • Strong analytical skillsintermediate
  • Strong scientific data and evidence interpretation and contextualizationintermediate
  • Ability to work effectively with cross-functional teams including clinical, commercialization, regulatory, HEOR and Accessintermediate
  • Entrepreneurial thinkingintermediate
  • Ability to anticipate needs, assess and manage business and organizational risksintermediate
  • Highly organized and motivatedintermediate
  • Excellent people management skillsintermediate
  • Excellent interpersonal skillsintermediate
  • Strong communication skillsintermediate
  • Proven ability to align across diverse teams and influence stakeholders toward shared successintermediate
  • Demonstrated capability to drive initiatives beyond effectiveness, ensuring measurable impact and resultsintermediate
  • Experience leading high-performing matrixed teams to deliver strategic outcomes and organizational impactintermediate
  • Strong track record of managing and developing talent with a focus on performance, engagement, and growthintermediate
  • Ability to anticipate market dynamics and identify opportunities to accelerate pipeline developmentintermediate

Required Qualifications

  • Advanced scientific degree (e.g., Pharm.D., MD, PhD) (experience)
  • 0+ years of experience (experience)
  • + years clinical trial expertise with a mix of development/clinical and medical with an emphasis on conduct/execution of trials (experience)

Preferred Qualifications

  • Formal specialization in areas associated with the current cell therapy portfolio (experience)
  • Professional experience with assets in cell therapy space (experience)

Responsibilities

  • Develop the 3-year strategic MEG plan for Cell Therapy
  • Provide oversight of the portfolio of studies and thought partnership on trade-offs across studies to the worldwide TA (WWTA) and HEOR partners
  • Drive the development and maintenance of the IEPs for the Cell Therapy assets/indications
  • Ensure alignment with unmet medical needs and business priorities in partnership with WWTA teams, HEOR, GDD and other key internal stakeholders
  • Overall end to end responsibility for the medical oversight of Cell Therapy MEG book of work
  • Ensure studies are on strategy and executed with rigor and on time
  • Serve as a matrix partner with CT Leadership Team, Global Medical and International Medical teams
  • Facilitate Medical governance through the TAG forum and support MEG leads in executing EGWG meetings
  • Foster an innovative culture and lead initiatives to increase innovative approaches to evidence generation
  • Leverage data analytics to define value drivers that will drive data-driven decisions
  • Provide scientific oversight and clinical decision-making responsibility for studies within remit
  • Ensure fiscal responsibility by maintaining a balanced budget for MEG Book of Work (BOW)
  • Chair the Review Committees or contribute during the approval process for final protocols, amendments, and budgets for studies under remit
  • Serve as the subject matter expert on the current book of work for studies under remit
  • Give updates to senior leadership/key stakeholders across the organization
  • Lead and mentor a team of MEG Leads, Clinical Scientists, Clinical Trial Physicians and project managers
  • Ensure strategic and rigorous execution of all scientific aspects associated with evidence generation activities
  • Serve as a trusted expert in meetings with investigators, external stakeholders and cross-functional internal teams
  • Discuss scientific rational and expected impact, challenges associated with execution, budget concerns, and/or data readouts

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
  • general: Programs supporting people with disabilities

Travel Requirements

0%

Target Your Resume for "Executive Director, Medical Evidence Generation Cell Therapy, Global Medical Affairs" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Executive Director, Medical Evidence Generation Cell Therapy, Global Medical Affairs. Takes only 15 seconds!

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

Check Your ATS Score for "Executive Director, Medical Evidence Generation Cell Therapy, Global Medical Affairs" , 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

Related Jobs You May Like

No related jobs found at the moment.