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Bristol-Myers Squibb logo

Senior Vice President, Global Development Operations

Bristol-Myers Squibb

Senior Vice President, Global Development Operations

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: December 4, 2025

Number of Vacancies: 1

Job Description

Member of the Drug Development Leadership Team, reporting to the Chief Medical Officer Anticipates & drives strategic evolution of GDO function and provides strong leadership and vision for the function and in the execution of clinical trials Manages, builds and leads global development operations function to execute and achieve functional responsibilities and program goals in compliance with GCP, ICH and other global regulatory requirements Provides comprehensive strategic leadership for 2,100+ multi-site organization across 40+ countries; including Regional Clinical Operations, Global Trial Management, Global Data Management and Trial Delivery Support. Optimizes clinical trial costs, CRO contracts as part of continued strategic value capture Accountable to deliver innovative digital solutions to optimize and accelerate the clinical trial process Collaborates with development heads to establish clear strategy & objectives for clinical trials and programs including estimation and articulation of risks/benefits Delivers on BMS Diversity Commitments by increasing patient voice and diversity in BMS-conducted clinical trials Maintains full GCP compliance and ensures the highest ethical standards of clinical trial and business conduct Ensures that all operations comply with local HR, health, safety, environmental/risk management legislation and GCP as well as with corporate compliance policies Identifies and grows the next generation of GDO and DD leaders in partnership with the rest of the DD Leadership Team Influences beyond area of responsibilities to drive innovation agenda by partnering with all relevant stakeholder groups incl. Research, GPS, Commercialization and supporting functions. Maintains global leadership and external reputation that attracts outstanding staff and commands respect of investigators to provide competitive superiority for BMS 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 Bachelor's degree in Science or Business, Advanced degree strongly preferred. Significant experience (20+years) of drug development or related experience managing clinical and CMC development under a variety of contexts; multiple clinical trials and operations required (ideally with pharma co and /or CRO) A demonstrated track record of success leading, engaging, managing, and developing a large global multi-site, multi-cultural organization Leadership experience of a large-scale enterprise transformation at global level, with a significant R&D component as a key driver (renewal of portfolio, development cycle. M&A activity) Ability to develop strong working relationships with key internal stakeholders and outside of BMS (functional and project leaders, peers and employees at all levels, vendors, Pharma industry community) Demonstrated ability to develop strategic direction for GDO in support of R&D strategy Strong scientific competency and credibility Excellent leadership capabilities: able to engage and inspire a fast-moving organization. Managing cross-geographic and complex organizations, processes, technology and talent Experience driving transformation across organizational changes, digital uplift and accelerating ways of working Experience having developed next generation leaders in previous assignments

About the Role/Company

  • Member of the Drug Development Leadership Team, reporting to the Chief Medical Officer
  • Part of Bristol Myers Squibb (BMS), a global biopharmaceutical company

Key Responsibilities

  • Anticipate and drive strategic evolution of GDO function
  • Provide strong leadership and vision for the function and execution of clinical trials
  • Manage, build, and lead global development operations function to achieve functional responsibilities and program goals
  • Ensure compliance with GCP, ICH, and other global regulatory requirements
  • Provide comprehensive strategic leadership for a multi-site organization across 40+ countries
  • Optimize clinical trial costs and CRO contracts
  • Deliver innovative digital solutions to optimize and accelerate the clinical trial process
  • Collaborate with development heads to establish clear strategy and objectives for clinical trials and programs
  • Estimate and articulate risks and benefits of clinical trials
  • Deliver on BMS Diversity Commitments by increasing patient voice and diversity in clinical trials
  • Maintain full GCP compliance and ensure the highest ethical standards of clinical trial and business conduct
  • Ensure compliance with local HR, health, safety, environmental/risk management legislation and corporate compliance policies
  • Identify and grow the next generation of GDO and DD leaders
  • Influence beyond area of responsibilities to drive innovation agenda by partnering with all relevant stakeholder groups
  • Maintain global leadership and external reputation to attract outstanding staff and command respect of investigators

Required Qualifications

  • Bachelor's degree in Science or Business
  • Advanced degree strongly preferred
  • Significant experience (20+ years) of drug development or related experience managing clinical and CMC development
  • Experience with multiple clinical trials and operations, ideally with pharmaceutical company and/or CRO
  • Leadership experience of a large-scale enterprise transformation at global level with a significant R&D component
  • Experience in portfolio renewal, development cycle, and M&A activity

Skills Required

  • Ability to develop strong working relationships with key internal and external stakeholders
  • Demonstrated ability to develop strategic direction for GDO in support of R&D strategy
  • Strong scientific competency and credibility
  • Excellent leadership capabilities to engage and inspire a fast-moving organization
  • Experience managing cross-geographic and complex organizations, processes, technology, and talent
  • Experience driving transformation across organizational changes, digital uplift, and accelerating ways of working
  • Experience in developing next generation leaders

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

Locations

  • Princeton NJ, United States
  • Madison Giralda NJ, United States
  • Boudry, United States
  • Cambridge MA, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

250,000 - 500,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Ability to develop strong working relationships with key internal and external stakeholdersintermediate
  • Demonstrated ability to develop strategic direction for GDO in support of R&D strategyintermediate
  • Strong scientific competency and credibilityintermediate
  • Excellent leadership capabilities to engage and inspire a fast-moving organizationintermediate
  • Experience managing cross-geographic and complex organizations, processes, technology, and talentintermediate
  • Experience driving transformation across organizational changes, digital uplift, and accelerating ways of workingintermediate
  • Experience in developing next generation leadersintermediate

Required Qualifications

  • Bachelor's degree in Science or Business (experience)
  • Advanced degree strongly preferred (experience)
  • Significant experience (20+ years) of drug development or related experience managing clinical and CMC development (experience)
  • Experience with multiple clinical trials and operations, ideally with pharmaceutical company and/or CRO (experience)
  • Leadership experience of a large-scale enterprise transformation at global level with a significant R&D component (experience)
  • Experience in portfolio renewal, development cycle, and M&A activity (experience)

Responsibilities

  • Anticipate and drive strategic evolution of GDO function
  • Provide strong leadership and vision for the function and execution of clinical trials
  • Manage, build, and lead global development operations function to achieve functional responsibilities and program goals
  • Ensure compliance with GCP, ICH, and other global regulatory requirements
  • Provide comprehensive strategic leadership for a multi-site organization across 40+ countries
  • Optimize clinical trial costs and CRO contracts
  • Deliver innovative digital solutions to optimize and accelerate the clinical trial process
  • Collaborate with development heads to establish clear strategy and objectives for clinical trials and programs
  • Estimate and articulate risks and benefits of clinical trials
  • Deliver on BMS Diversity Commitments by increasing patient voice and diversity in clinical trials
  • Maintain full GCP compliance and ensure the highest ethical standards of clinical trial and business conduct
  • Ensure compliance with local HR, health, safety, environmental/risk management legislation and corporate compliance policies
  • Identify and grow the next generation of GDO and DD leaders
  • Influence beyond area of responsibilities to drive innovation agenda by partnering with all relevant stakeholder groups
  • Maintain global leadership and external reputation to attract outstanding staff and command respect of investigators

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

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Bristol-Myers Squibb logo

Senior Vice President, Global Development Operations

Bristol-Myers Squibb

Senior Vice President, Global Development Operations

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: December 4, 2025

Number of Vacancies: 1

Job Description

Member of the Drug Development Leadership Team, reporting to the Chief Medical Officer Anticipates & drives strategic evolution of GDO function and provides strong leadership and vision for the function and in the execution of clinical trials Manages, builds and leads global development operations function to execute and achieve functional responsibilities and program goals in compliance with GCP, ICH and other global regulatory requirements Provides comprehensive strategic leadership for 2,100+ multi-site organization across 40+ countries; including Regional Clinical Operations, Global Trial Management, Global Data Management and Trial Delivery Support. Optimizes clinical trial costs, CRO contracts as part of continued strategic value capture Accountable to deliver innovative digital solutions to optimize and accelerate the clinical trial process Collaborates with development heads to establish clear strategy & objectives for clinical trials and programs including estimation and articulation of risks/benefits Delivers on BMS Diversity Commitments by increasing patient voice and diversity in BMS-conducted clinical trials Maintains full GCP compliance and ensures the highest ethical standards of clinical trial and business conduct Ensures that all operations comply with local HR, health, safety, environmental/risk management legislation and GCP as well as with corporate compliance policies Identifies and grows the next generation of GDO and DD leaders in partnership with the rest of the DD Leadership Team Influences beyond area of responsibilities to drive innovation agenda by partnering with all relevant stakeholder groups incl. Research, GPS, Commercialization and supporting functions. Maintains global leadership and external reputation that attracts outstanding staff and commands respect of investigators to provide competitive superiority for BMS 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 Bachelor's degree in Science or Business, Advanced degree strongly preferred. Significant experience (20+years) of drug development or related experience managing clinical and CMC development under a variety of contexts; multiple clinical trials and operations required (ideally with pharma co and /or CRO) A demonstrated track record of success leading, engaging, managing, and developing a large global multi-site, multi-cultural organization Leadership experience of a large-scale enterprise transformation at global level, with a significant R&D component as a key driver (renewal of portfolio, development cycle. M&A activity) Ability to develop strong working relationships with key internal stakeholders and outside of BMS (functional and project leaders, peers and employees at all levels, vendors, Pharma industry community) Demonstrated ability to develop strategic direction for GDO in support of R&D strategy Strong scientific competency and credibility Excellent leadership capabilities: able to engage and inspire a fast-moving organization. Managing cross-geographic and complex organizations, processes, technology and talent Experience driving transformation across organizational changes, digital uplift and accelerating ways of working Experience having developed next generation leaders in previous assignments

About the Role/Company

  • Member of the Drug Development Leadership Team, reporting to the Chief Medical Officer
  • Part of Bristol Myers Squibb (BMS), a global biopharmaceutical company

Key Responsibilities

  • Anticipate and drive strategic evolution of GDO function
  • Provide strong leadership and vision for the function and execution of clinical trials
  • Manage, build, and lead global development operations function to achieve functional responsibilities and program goals
  • Ensure compliance with GCP, ICH, and other global regulatory requirements
  • Provide comprehensive strategic leadership for a multi-site organization across 40+ countries
  • Optimize clinical trial costs and CRO contracts
  • Deliver innovative digital solutions to optimize and accelerate the clinical trial process
  • Collaborate with development heads to establish clear strategy and objectives for clinical trials and programs
  • Estimate and articulate risks and benefits of clinical trials
  • Deliver on BMS Diversity Commitments by increasing patient voice and diversity in clinical trials
  • Maintain full GCP compliance and ensure the highest ethical standards of clinical trial and business conduct
  • Ensure compliance with local HR, health, safety, environmental/risk management legislation and corporate compliance policies
  • Identify and grow the next generation of GDO and DD leaders
  • Influence beyond area of responsibilities to drive innovation agenda by partnering with all relevant stakeholder groups
  • Maintain global leadership and external reputation to attract outstanding staff and command respect of investigators

Required Qualifications

  • Bachelor's degree in Science or Business
  • Advanced degree strongly preferred
  • Significant experience (20+ years) of drug development or related experience managing clinical and CMC development
  • Experience with multiple clinical trials and operations, ideally with pharmaceutical company and/or CRO
  • Leadership experience of a large-scale enterprise transformation at global level with a significant R&D component
  • Experience in portfolio renewal, development cycle, and M&A activity

Skills Required

  • Ability to develop strong working relationships with key internal and external stakeholders
  • Demonstrated ability to develop strategic direction for GDO in support of R&D strategy
  • Strong scientific competency and credibility
  • Excellent leadership capabilities to engage and inspire a fast-moving organization
  • Experience managing cross-geographic and complex organizations, processes, technology, and talent
  • Experience driving transformation across organizational changes, digital uplift, and accelerating ways of working
  • Experience in developing next generation leaders

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

Locations

  • Princeton NJ, United States
  • Madison Giralda NJ, United States
  • Boudry, United States
  • Cambridge MA, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

250,000 - 500,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Ability to develop strong working relationships with key internal and external stakeholdersintermediate
  • Demonstrated ability to develop strategic direction for GDO in support of R&D strategyintermediate
  • Strong scientific competency and credibilityintermediate
  • Excellent leadership capabilities to engage and inspire a fast-moving organizationintermediate
  • Experience managing cross-geographic and complex organizations, processes, technology, and talentintermediate
  • Experience driving transformation across organizational changes, digital uplift, and accelerating ways of workingintermediate
  • Experience in developing next generation leadersintermediate

Required Qualifications

  • Bachelor's degree in Science or Business (experience)
  • Advanced degree strongly preferred (experience)
  • Significant experience (20+ years) of drug development or related experience managing clinical and CMC development (experience)
  • Experience with multiple clinical trials and operations, ideally with pharmaceutical company and/or CRO (experience)
  • Leadership experience of a large-scale enterprise transformation at global level with a significant R&D component (experience)
  • Experience in portfolio renewal, development cycle, and M&A activity (experience)

Responsibilities

  • Anticipate and drive strategic evolution of GDO function
  • Provide strong leadership and vision for the function and execution of clinical trials
  • Manage, build, and lead global development operations function to achieve functional responsibilities and program goals
  • Ensure compliance with GCP, ICH, and other global regulatory requirements
  • Provide comprehensive strategic leadership for a multi-site organization across 40+ countries
  • Optimize clinical trial costs and CRO contracts
  • Deliver innovative digital solutions to optimize and accelerate the clinical trial process
  • Collaborate with development heads to establish clear strategy and objectives for clinical trials and programs
  • Estimate and articulate risks and benefits of clinical trials
  • Deliver on BMS Diversity Commitments by increasing patient voice and diversity in clinical trials
  • Maintain full GCP compliance and ensure the highest ethical standards of clinical trial and business conduct
  • Ensure compliance with local HR, health, safety, environmental/risk management legislation and corporate compliance policies
  • Identify and grow the next generation of GDO and DD leaders
  • Influence beyond area of responsibilities to drive innovation agenda by partnering with all relevant stakeholder groups
  • Maintain global leadership and external reputation to attract outstanding staff and command respect of investigators

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

Target Your Resume for "Senior Vice President, Global Development Operations" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Senior Vice President, Global Development Operations. Takes only 15 seconds!

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

Check Your ATS Score for "Senior Vice President, Global Development Operations" , 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

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