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Senior Global Trial Lead

Bristol-Myers Squibb

Healthcare Jobs

Senior Global Trial Lead

full-timePosted: Oct 28, 2025

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. Shape the Future of Clinical Trials with Us Join Our Global Development Team! Are you ready to drive impactful change in clinical research? We're seeking a passionate and experienced Senior Global Trial Lead (GTL) to lead the strategic and operational delivery of global clinical trials within our Global Development Operations team. This high-visibility role offers you the opportunity to influence study outcomes, collaborate across continents, and make a meaningful difference in patient lives. Position office based in Poland - Warsaw. What You'll Do: Lead Global Trials: Oversee the planning and execution of international clinical studies from start to finish, ensuring excellence in timelines, quality, and regulatory compliance. Drive Project Success: Collaborate with cross-functional teams, vendors, and stakeholders to achieve study milestones and resolve challenges proactively. Strategic Oversight: Guide operational strategy, manage risks, and optimize budgets while upholding the highest standards of data integrity and patient safety. Mentor & Inspire: Support and mentor team members, fostering a culture of collaboration, growth, and innovation. Shape the Future: Influence global best practices and contribute to organizational decision-making on study and portfolio levels. What We're Looking For: Bachelor's degree or higher in a relevant field. Therapeutic Area Eperience in Cardiovascular, Immunology, Neurology, Oncology, Cell Therapy is a plus 6+ years of experience in clinical operations and project management within the pharmaceutical or healthcare industry, including multi-national trial leadership. Proven ability to lead complex, global, multi-functional teams in a matrixed environment. Expertise in vendor management, budget oversight, and regulatory compliance. Strong communication, critical thinking, and collaboration skills. Ability to travel up to 25% globally as needed. Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned. Why Join Us? Be a key leader in global studies impacting diverse therapeutic areas. Work with talented teams across the US, India, Switzerland, and beyond. Grow your career in a supportive, forward-thinking environment. Make your mark in delivering high-quality, innovative clinical solutions. Ready to take your leadership to the next level? Apply now and help us shape the next generation of global clinical trials! 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. We kindly ask all applicants to send their CV in English. 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. 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. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. 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/ 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 uniquely interesting work happens every day, transforming the lives of patients and the careers of employees
  • The company offers opportunities for growth and career advancement alongside high-achieving teams
  • BMS emphasizes balance and flexibility in the work environment
  • BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process and reasonable workplace accommodations
  • BMS strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters
  • BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws

Key Responsibilities

  • Oversee the planning and execution of international clinical studies from start to finish, ensuring excellence in timelines, quality, and regulatory compliance
  • Collaborate with cross-functional teams, vendors, and stakeholders to achieve study milestones and resolve challenges proactively
  • Guide operational strategy, manage risks, and optimize budgets while upholding the highest standards of data integrity and patient safety
  • Support and mentor team members, fostering a culture of collaboration, growth, and innovation
  • Influence global best practices and contribute to organizational decision-making on study and portfolio levels

Required Qualifications

  • Bachelor's degree or higher in a relevant field
  • + years of experience in clinical operations and project management within the pharmaceutical or healthcare industry
  • Experience in multi-national trial leadership
  • Proven ability to lead complex, global, multi-functional teams in a matrixed environment
  • Expertise in vendor management, budget oversight, and regulatory compliance

Preferred Qualifications

  • Therapeutic Area Experience in Cardiovascular, Immunology, Neurology, Oncology, Cell Therapy

Skills Required

  • Strong communication skills
  • Critical thinking
  • Collaboration skills
  • Ability to influence study outcomes and collaborate across continents

Benefits & Perks

  • Competitive benefits, services, and programs
  • Opportunity to discuss remote work up to 50% of the time over a two-week period
  • Supportive, forward-thinking work environment
  • Opportunity to grow and thrive through uncommon opportunities in scale and scope

Additional Requirements

  • Ability to travel up to 25% globally as needed
  • Position office based in Poland - Warsaw
  • CV must be sent in English
  • On-site presence is considered an essential job function for site-by-design roles, requiring at least 50% onsite at the assigned facility

Locations

  • Warsaw, United States
  • Warszawa, Mazowieckie, PL, United States
  • Warszawa, United States

Salary

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
  • Collaboration skillsintermediate
  • Ability to influence study outcomes and collaborate across continentsintermediate

Required Qualifications

  • Bachelor's degree or higher in a relevant field (experience)
  • + years of experience in clinical operations and project management within the pharmaceutical or healthcare industry (experience)
  • Experience in multi-national trial leadership (experience)
  • Proven ability to lead complex, global, multi-functional teams in a matrixed environment (experience)
  • Expertise in vendor management, budget oversight, and regulatory compliance (experience)

Preferred Qualifications

  • Therapeutic Area Experience in Cardiovascular, Immunology, Neurology, Oncology, Cell Therapy (experience)

Responsibilities

  • Oversee the planning and execution of international clinical studies from start to finish, ensuring excellence in timelines, quality, and regulatory compliance
  • Collaborate with cross-functional teams, vendors, and stakeholders to achieve study milestones and resolve challenges proactively
  • Guide operational strategy, manage risks, and optimize budgets while upholding the highest standards of data integrity and patient safety
  • Support and mentor team members, fostering a culture of collaboration, growth, and innovation
  • Influence global best practices and contribute to organizational decision-making on study and portfolio levels

Benefits

  • general: Competitive benefits, services, and programs
  • general: Opportunity to discuss remote work up to 50% of the time over a two-week period
  • general: Supportive, forward-thinking work environment
  • general: Opportunity to grow and thrive through uncommon opportunities in scale and scope

Travel Requirements

5%

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Bristol-Myers Squibb logo

Senior Global Trial Lead

Bristol-Myers Squibb

Healthcare Jobs

Senior Global Trial Lead

full-timePosted: Oct 28, 2025

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. Shape the Future of Clinical Trials with Us Join Our Global Development Team! Are you ready to drive impactful change in clinical research? We're seeking a passionate and experienced Senior Global Trial Lead (GTL) to lead the strategic and operational delivery of global clinical trials within our Global Development Operations team. This high-visibility role offers you the opportunity to influence study outcomes, collaborate across continents, and make a meaningful difference in patient lives. Position office based in Poland - Warsaw. What You'll Do: Lead Global Trials: Oversee the planning and execution of international clinical studies from start to finish, ensuring excellence in timelines, quality, and regulatory compliance. Drive Project Success: Collaborate with cross-functional teams, vendors, and stakeholders to achieve study milestones and resolve challenges proactively. Strategic Oversight: Guide operational strategy, manage risks, and optimize budgets while upholding the highest standards of data integrity and patient safety. Mentor & Inspire: Support and mentor team members, fostering a culture of collaboration, growth, and innovation. Shape the Future: Influence global best practices and contribute to organizational decision-making on study and portfolio levels. What We're Looking For: Bachelor's degree or higher in a relevant field. Therapeutic Area Eperience in Cardiovascular, Immunology, Neurology, Oncology, Cell Therapy is a plus 6+ years of experience in clinical operations and project management within the pharmaceutical or healthcare industry, including multi-national trial leadership. Proven ability to lead complex, global, multi-functional teams in a matrixed environment. Expertise in vendor management, budget oversight, and regulatory compliance. Strong communication, critical thinking, and collaboration skills. Ability to travel up to 25% globally as needed. Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned. Why Join Us? Be a key leader in global studies impacting diverse therapeutic areas. Work with talented teams across the US, India, Switzerland, and beyond. Grow your career in a supportive, forward-thinking environment. Make your mark in delivering high-quality, innovative clinical solutions. Ready to take your leadership to the next level? Apply now and help us shape the next generation of global clinical trials! 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. We kindly ask all applicants to send their CV in English. 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. 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. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. 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/ 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 uniquely interesting work happens every day, transforming the lives of patients and the careers of employees
  • The company offers opportunities for growth and career advancement alongside high-achieving teams
  • BMS emphasizes balance and flexibility in the work environment
  • BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process and reasonable workplace accommodations
  • BMS strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters
  • BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws

Key Responsibilities

  • Oversee the planning and execution of international clinical studies from start to finish, ensuring excellence in timelines, quality, and regulatory compliance
  • Collaborate with cross-functional teams, vendors, and stakeholders to achieve study milestones and resolve challenges proactively
  • Guide operational strategy, manage risks, and optimize budgets while upholding the highest standards of data integrity and patient safety
  • Support and mentor team members, fostering a culture of collaboration, growth, and innovation
  • Influence global best practices and contribute to organizational decision-making on study and portfolio levels

Required Qualifications

  • Bachelor's degree or higher in a relevant field
  • + years of experience in clinical operations and project management within the pharmaceutical or healthcare industry
  • Experience in multi-national trial leadership
  • Proven ability to lead complex, global, multi-functional teams in a matrixed environment
  • Expertise in vendor management, budget oversight, and regulatory compliance

Preferred Qualifications

  • Therapeutic Area Experience in Cardiovascular, Immunology, Neurology, Oncology, Cell Therapy

Skills Required

  • Strong communication skills
  • Critical thinking
  • Collaboration skills
  • Ability to influence study outcomes and collaborate across continents

Benefits & Perks

  • Competitive benefits, services, and programs
  • Opportunity to discuss remote work up to 50% of the time over a two-week period
  • Supportive, forward-thinking work environment
  • Opportunity to grow and thrive through uncommon opportunities in scale and scope

Additional Requirements

  • Ability to travel up to 25% globally as needed
  • Position office based in Poland - Warsaw
  • CV must be sent in English
  • On-site presence is considered an essential job function for site-by-design roles, requiring at least 50% onsite at the assigned facility

Locations

  • Warsaw, United States
  • Warszawa, Mazowieckie, PL, United States
  • Warszawa, United States

Salary

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
  • Collaboration skillsintermediate
  • Ability to influence study outcomes and collaborate across continentsintermediate

Required Qualifications

  • Bachelor's degree or higher in a relevant field (experience)
  • + years of experience in clinical operations and project management within the pharmaceutical or healthcare industry (experience)
  • Experience in multi-national trial leadership (experience)
  • Proven ability to lead complex, global, multi-functional teams in a matrixed environment (experience)
  • Expertise in vendor management, budget oversight, and regulatory compliance (experience)

Preferred Qualifications

  • Therapeutic Area Experience in Cardiovascular, Immunology, Neurology, Oncology, Cell Therapy (experience)

Responsibilities

  • Oversee the planning and execution of international clinical studies from start to finish, ensuring excellence in timelines, quality, and regulatory compliance
  • Collaborate with cross-functional teams, vendors, and stakeholders to achieve study milestones and resolve challenges proactively
  • Guide operational strategy, manage risks, and optimize budgets while upholding the highest standards of data integrity and patient safety
  • Support and mentor team members, fostering a culture of collaboration, growth, and innovation
  • Influence global best practices and contribute to organizational decision-making on study and portfolio levels

Benefits

  • general: Competitive benefits, services, and programs
  • general: Opportunity to discuss remote work up to 50% of the time over a two-week period
  • general: Supportive, forward-thinking work environment
  • general: Opportunity to grow and thrive through uncommon opportunities in scale and scope

Travel Requirements

5%

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

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

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

Check Your ATS Score for "Senior Global Trial Lead" , 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

Answer 10 quick questions to check your fit for Senior Global Trial Lead @ Bristol-Myers Squibb.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.