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Director, Global Trial Lead(m/w/x)
Leading complex multi-national clinical trials at a science-driven organization, ensuring data quality and regulatory compliance. 10+ years in clinical operations and global project management, with Director-level global trial leadership, required. Strategic leadership for global clinical programs.
Requirements
- Advanced degree (MS, PharmD, PhD, MD, or equivalent) preferred
- BA/BS required
- Minimum 10 years of experience in clinical operations and global project management
- Multi-national experience
- Experience in leading global clinical trials and programs at the Director level
- Experience leading global and multi-functional study teams
- Experience in managing CROs and external partners at a strategic level preferred
- Proficiency in AI tools and familiarity with technological advancements preferred
- Travel requirement: up to 25%
- Ability to physically travel to visit customers, patients or business partners
Tasks
- Provide leadership for complex clinical trials
- Ensure delivery of high-quality data and regulatory compliance
- Collaborate with internal teams and vendors for trial delivery
- Oversee operational activities and study feasibility
- Make decisions on complex issues and manage risks
- Manage study budgets, contracts, and scope of work
- Participate in vendor selection and evaluation
- Oversee vendor relationships and ensure alignment
- Set and monitor performance metrics for trials
- Utilize quality indicators to optimize trial execution
- Maintain accurate data records in study management systems
- Establish project management tools for studies
- Develop trial-specific standards for operational consistency
- Lead organizational change initiatives and best practices
- Foster cross-functional collaboration for knowledge sharing
- Champion innovative solutions for trial acceleration
- Define strategic direction for clinical trial execution
- Provide guidance on study protocols and execution strategies
- Monitor trends in clinical operations and advise teams
- Mentor GDO Study Team members and future leaders
- Promote a high-performing team culture and collaboration
- Model ethical behavior and commitment to learning
- Drive upfront planning of study timelines and budgets
- Lead quarterly budget reviews and flag variances
- Approve and reconcile vendor invoices and amendments
- Identify and resolve budget and timeline issues
- Manage study logistics and escalate resourcing needs
- Oversee execution of multiple clinical trials
- Provide lifecycle leadership from start-up to close-out
- Analyze operational metrics for study optimization
- Identify challenges and propose actionable solutions
- Build partnerships with internal and external stakeholders
- Lead global clinical trials with strategic oversight
- Ensure compliance with regulatory standards and patient safety
- Manage end-to-end trial operations and resource planning
- Mitigate risks to ensure trial continuity and delivery
- Demonstrate diplomacy in interfacing with stakeholders
- Utilize clinical systems to track milestones and data quality
- Lead large cross-functional teams toward shared goals
- Support mentoring of new GTL team members
- Exhibit critical thinking and problem-solving skills
- Make informed decisions in high-pressure environments
- Communicate effectively with cross-functional teams
- Build trust-based relationships with diverse stakeholders
Work Experience
- 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- AI tools
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Director, Global Trial Lead(m/w/x)
Leading complex multi-national clinical trials at a science-driven organization, ensuring data quality and regulatory compliance. 10+ years in clinical operations and global project management, with Director-level global trial leadership, required. Strategic leadership for global clinical programs.
Requirements
- Advanced degree (MS, PharmD, PhD, MD, or equivalent) preferred
- BA/BS required
- Minimum 10 years of experience in clinical operations and global project management
- Multi-national experience
- Experience in leading global clinical trials and programs at the Director level
- Experience leading global and multi-functional study teams
- Experience in managing CROs and external partners at a strategic level preferred
- Proficiency in AI tools and familiarity with technological advancements preferred
- Travel requirement: up to 25%
- Ability to physically travel to visit customers, patients or business partners
Tasks
- Provide leadership for complex clinical trials
- Ensure delivery of high-quality data and regulatory compliance
- Collaborate with internal teams and vendors for trial delivery
- Oversee operational activities and study feasibility
- Make decisions on complex issues and manage risks
- Manage study budgets, contracts, and scope of work
- Participate in vendor selection and evaluation
- Oversee vendor relationships and ensure alignment
- Set and monitor performance metrics for trials
- Utilize quality indicators to optimize trial execution
- Maintain accurate data records in study management systems
- Establish project management tools for studies
- Develop trial-specific standards for operational consistency
- Lead organizational change initiatives and best practices
- Foster cross-functional collaboration for knowledge sharing
- Champion innovative solutions for trial acceleration
- Define strategic direction for clinical trial execution
- Provide guidance on study protocols and execution strategies
- Monitor trends in clinical operations and advise teams
- Mentor GDO Study Team members and future leaders
- Promote a high-performing team culture and collaboration
- Model ethical behavior and commitment to learning
- Drive upfront planning of study timelines and budgets
- Lead quarterly budget reviews and flag variances
- Approve and reconcile vendor invoices and amendments
- Identify and resolve budget and timeline issues
- Manage study logistics and escalate resourcing needs
- Oversee execution of multiple clinical trials
- Provide lifecycle leadership from start-up to close-out
- Analyze operational metrics for study optimization
- Identify challenges and propose actionable solutions
- Build partnerships with internal and external stakeholders
- Lead global clinical trials with strategic oversight
- Ensure compliance with regulatory standards and patient safety
- Manage end-to-end trial operations and resource planning
- Mitigate risks to ensure trial continuity and delivery
- Demonstrate diplomacy in interfacing with stakeholders
- Utilize clinical systems to track milestones and data quality
- Lead large cross-functional teams toward shared goals
- Support mentoring of new GTL team members
- Exhibit critical thinking and problem-solving skills
- Make informed decisions in high-pressure environments
- Communicate effectively with cross-functional teams
- Build trust-based relationships with diverse stakeholders
Work Experience
- 10 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- AI tools
About the Company
Bristol Myers Squibb
Industry
Pharmaceuticals
Description
The company is dedicated to transforming patients’ lives through science and promotes global participation in clinical trials.
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- Bristol Myers Squibb
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