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Bristol-Myers Squibb logo

Global Trial Lead - Clinical Pharmacology

Bristol-Myers Squibb

Global Trial Lead - Clinical Pharmacology

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 24, 2025

Number of Vacancies: 1

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. 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. Join Our Global Development Operations Team! Are you ready to make a significant impact in clinical research on a global scale? We're seeking a passionate Global Trial Lead (GTL) with focus on Clinical Pharmacology to join our dynamic Global Development Operations (GDO) team. In this office based position in Poland - Warsaw, you'll lead the execution of critical clinical trials and champion operational excellence across diverse therapeutic areas. Your Impact: Leadership: Guide cross-functional teams and vendors to deliver clinical trials on time, within budget, and in full compliance with regulatory standards. Strategy & Execution: Shape study-level strategies, drive operational alignment, and proactively resolve risks and issues. Collaboration: Build strong partnerships with internal stakeholders and external collaborators to optimize study outcomes. Innovation: Lead global initiatives, support portfolio-level inquiries, and influence decision-making at both study and organizational levels. What You'll Do: Lead and oversee global clinical trials from start-up to close-out, ensuring excellence in delivery and compliance. Develop and manage project plans, budgets, and resources, including vendor relationships and performance metrics. Provide strategic input on study feasibility and operational activities. Identify and proactively manage risks, balancing cost, deliverables, and quality. Foster an inclusive, collaborative, and high-performing team environment. Maintain accurate data records in study management systems (e.g., CTMS, eTMF). What We're Looking For Bachelor's degree (BA/BS) or equivalent in a relevant field. Minimum 4 years' experience in clinical operations and project management, including multi-national trial leadership. Experience with Clinical Pharmacology preferred Proven expertise in leading global clinical trials and teams. Strong communication, critical thinking, and stakeholder engagement skills. Experience in managing CROs and vendors preferred. Up to 25% travel may be required. Why Join Us? Make a global impact, grow your career, and work with passionate professionals dedicated to transforming patient care through clinical research. If you thrive in a fast-paced, collaborative, and diverse environment, we want to hear from you! Ready to drive the future of clinical development? Apply today and help us deliver life-changing therapies to patients worldwide. Based on your function, department or individual position, you will have the opportunity to discuss with your Manager the option to work remotely up to 50% of the time, over a two-week period, with the flexibility to choose the days that align with your collaboration needs. LI-Hybrid If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. 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: 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 adastaffingsupport@bms.com. 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.

About the Role/Company

  • Bristol Myers Squibb is a company where challenging, meaningful, and life-changing work happens every day
  • The company offers opportunities for growth and career development
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in the work environment
  • The Global Development Operations (GDO) team is dynamic and focused on clinical research on a global scale
  • BMS is dedicated to transforming patient care through clinical research
  • BMS promotes a supportive culture with shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • BMS is committed to ensuring people with disabilities can excel through a transparent recruitment process and reasonable workplace accommodations

Key Responsibilities

  • Lead and oversee global clinical trials from start-up to close-out, ensuring excellence in delivery and compliance
  • Develop and manage project plans, budgets, and resources, including vendor relationships and performance metrics
  • Provide strategic input on study feasibility and operational activities
  • Identify and proactively manage risks, balancing cost, deliverables, and quality
  • Foster an inclusive, collaborative, and high-performing team environment
  • Maintain accurate data records in study management systems (e.g., CTMS, eTMF)
  • Guide cross-functional teams and vendors to deliver clinical trials on time, within budget, and in full compliance with regulatory standards
  • Shape study-level strategies, drive operational alignment, and proactively resolve risks and issues
  • Build strong partnerships with internal stakeholders and external collaborators to optimize study outcomes
  • Lead global initiatives, support portfolio-level inquiries, and influence decision-making at both study and organizational levels

Required Qualifications

  • Bachelor's degree (BA/BS) or equivalent in a relevant field
  • Minimum 4 years' experience in clinical operations and project management
  • Experience in multi-national trial leadership

Preferred Qualifications

  • Experience with Clinical Pharmacology
  • Experience in managing CROs and vendors

Skills Required

  • Strong communication skills
  • Critical thinking
  • Stakeholder engagement skills
  • Proven expertise in leading global clinical trials and teams

Benefits & Perks

  • Competitive benefits, services, and programs
  • Opportunity to discuss remote work up to 50% of the time
  • Flexibility to choose work days that align with collaboration needs

Additional Requirements

  • Up to 25% travel may be required
  • Office-based position in Poland - Warsaw

Locations

  • Warsaw, United States

Salary

Salary not disclosed

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

  • Strong communication skillsintermediate
  • Critical thinkingintermediate
  • Stakeholder engagement skillsintermediate
  • Proven expertise in leading global clinical trials and teamsintermediate

Required Qualifications

  • Bachelor's degree (BA/BS) or equivalent in a relevant field (experience)
  • Minimum 4 years' experience in clinical operations and project management (experience)
  • Experience in multi-national trial leadership (experience)

Preferred Qualifications

  • Experience with Clinical Pharmacology (experience)
  • Experience in managing CROs and vendors (experience)

Responsibilities

  • Lead and oversee global clinical trials from start-up to close-out, ensuring excellence in delivery and compliance
  • Develop and manage project plans, budgets, and resources, including vendor relationships and performance metrics
  • Provide strategic input on study feasibility and operational activities
  • Identify and proactively manage risks, balancing cost, deliverables, and quality
  • Foster an inclusive, collaborative, and high-performing team environment
  • Maintain accurate data records in study management systems (e.g., CTMS, eTMF)
  • Guide cross-functional teams and vendors to deliver clinical trials on time, within budget, and in full compliance with regulatory standards
  • Shape study-level strategies, drive operational alignment, and proactively resolve risks and issues
  • Build strong partnerships with internal stakeholders and external collaborators to optimize study outcomes
  • Lead global initiatives, support portfolio-level inquiries, and influence decision-making at both study and organizational levels

Benefits

  • general: Competitive benefits, services, and programs
  • general: Opportunity to discuss remote work up to 50% of the time
  • general: Flexibility to choose work days that align with collaboration needs

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Bristol-Myers Squibb logo

Global Trial Lead - Clinical Pharmacology

Bristol-Myers Squibb

Global Trial Lead - Clinical Pharmacology

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 24, 2025

Number of Vacancies: 1

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. 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. Join Our Global Development Operations Team! Are you ready to make a significant impact in clinical research on a global scale? We're seeking a passionate Global Trial Lead (GTL) with focus on Clinical Pharmacology to join our dynamic Global Development Operations (GDO) team. In this office based position in Poland - Warsaw, you'll lead the execution of critical clinical trials and champion operational excellence across diverse therapeutic areas. Your Impact: Leadership: Guide cross-functional teams and vendors to deliver clinical trials on time, within budget, and in full compliance with regulatory standards. Strategy & Execution: Shape study-level strategies, drive operational alignment, and proactively resolve risks and issues. Collaboration: Build strong partnerships with internal stakeholders and external collaborators to optimize study outcomes. Innovation: Lead global initiatives, support portfolio-level inquiries, and influence decision-making at both study and organizational levels. What You'll Do: Lead and oversee global clinical trials from start-up to close-out, ensuring excellence in delivery and compliance. Develop and manage project plans, budgets, and resources, including vendor relationships and performance metrics. Provide strategic input on study feasibility and operational activities. Identify and proactively manage risks, balancing cost, deliverables, and quality. Foster an inclusive, collaborative, and high-performing team environment. Maintain accurate data records in study management systems (e.g., CTMS, eTMF). What We're Looking For Bachelor's degree (BA/BS) or equivalent in a relevant field. Minimum 4 years' experience in clinical operations and project management, including multi-national trial leadership. Experience with Clinical Pharmacology preferred Proven expertise in leading global clinical trials and teams. Strong communication, critical thinking, and stakeholder engagement skills. Experience in managing CROs and vendors preferred. Up to 25% travel may be required. Why Join Us? Make a global impact, grow your career, and work with passionate professionals dedicated to transforming patient care through clinical research. If you thrive in a fast-paced, collaborative, and diverse environment, we want to hear from you! Ready to drive the future of clinical development? Apply today and help us deliver life-changing therapies to patients worldwide. Based on your function, department or individual position, you will have the opportunity to discuss with your Manager the option to work remotely up to 50% of the time, over a two-week period, with the flexibility to choose the days that align with your collaboration needs. LI-Hybrid If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. 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: 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 adastaffingsupport@bms.com. 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.

About the Role/Company

  • Bristol Myers Squibb is a company where challenging, meaningful, and life-changing work happens every day
  • The company offers opportunities for growth and career development
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in the work environment
  • The Global Development Operations (GDO) team is dynamic and focused on clinical research on a global scale
  • BMS is dedicated to transforming patient care through clinical research
  • BMS promotes a supportive culture with shared values of passion, innovation, urgency, accountability, inclusion, and integrity
  • BMS is committed to ensuring people with disabilities can excel through a transparent recruitment process and reasonable workplace accommodations

Key Responsibilities

  • Lead and oversee global clinical trials from start-up to close-out, ensuring excellence in delivery and compliance
  • Develop and manage project plans, budgets, and resources, including vendor relationships and performance metrics
  • Provide strategic input on study feasibility and operational activities
  • Identify and proactively manage risks, balancing cost, deliverables, and quality
  • Foster an inclusive, collaborative, and high-performing team environment
  • Maintain accurate data records in study management systems (e.g., CTMS, eTMF)
  • Guide cross-functional teams and vendors to deliver clinical trials on time, within budget, and in full compliance with regulatory standards
  • Shape study-level strategies, drive operational alignment, and proactively resolve risks and issues
  • Build strong partnerships with internal stakeholders and external collaborators to optimize study outcomes
  • Lead global initiatives, support portfolio-level inquiries, and influence decision-making at both study and organizational levels

Required Qualifications

  • Bachelor's degree (BA/BS) or equivalent in a relevant field
  • Minimum 4 years' experience in clinical operations and project management
  • Experience in multi-national trial leadership

Preferred Qualifications

  • Experience with Clinical Pharmacology
  • Experience in managing CROs and vendors

Skills Required

  • Strong communication skills
  • Critical thinking
  • Stakeholder engagement skills
  • Proven expertise in leading global clinical trials and teams

Benefits & Perks

  • Competitive benefits, services, and programs
  • Opportunity to discuss remote work up to 50% of the time
  • Flexibility to choose work days that align with collaboration needs

Additional Requirements

  • Up to 25% travel may be required
  • Office-based position in Poland - Warsaw

Locations

  • Warsaw, United States

Salary

Salary not disclosed

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

  • Strong communication skillsintermediate
  • Critical thinkingintermediate
  • Stakeholder engagement skillsintermediate
  • Proven expertise in leading global clinical trials and teamsintermediate

Required Qualifications

  • Bachelor's degree (BA/BS) or equivalent in a relevant field (experience)
  • Minimum 4 years' experience in clinical operations and project management (experience)
  • Experience in multi-national trial leadership (experience)

Preferred Qualifications

  • Experience with Clinical Pharmacology (experience)
  • Experience in managing CROs and vendors (experience)

Responsibilities

  • Lead and oversee global clinical trials from start-up to close-out, ensuring excellence in delivery and compliance
  • Develop and manage project plans, budgets, and resources, including vendor relationships and performance metrics
  • Provide strategic input on study feasibility and operational activities
  • Identify and proactively manage risks, balancing cost, deliverables, and quality
  • Foster an inclusive, collaborative, and high-performing team environment
  • Maintain accurate data records in study management systems (e.g., CTMS, eTMF)
  • Guide cross-functional teams and vendors to deliver clinical trials on time, within budget, and in full compliance with regulatory standards
  • Shape study-level strategies, drive operational alignment, and proactively resolve risks and issues
  • Build strong partnerships with internal stakeholders and external collaborators to optimize study outcomes
  • Lead global initiatives, support portfolio-level inquiries, and influence decision-making at both study and organizational levels

Benefits

  • general: Competitive benefits, services, and programs
  • general: Opportunity to discuss remote work up to 50% of the time
  • general: Flexibility to choose work days that align with collaboration needs

Target Your Resume for "Global Trial Lead - Clinical Pharmacology" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Global Trial Lead - Clinical Pharmacology. Takes only 15 seconds!

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

Check Your ATS Score for "Global Trial Lead - Clinical Pharmacology" , 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.