Associate Director, Global Trial Lead
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Posted on:
24-10-2025
Vacancies:
1 Vacancy
Job Summary
Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: the Future of Clinical Trials with Us Are you ready to play a pivotal role in advancing clinical research around the world Were seeking an experienced Associate Director Global Trial Lead (GTL) to join our dynamic Global Development Operations team. Position office based in Poland - Warsaw youll lead critical global clinical trials and drive innovation in research and development. Leadership: Guide multi-functional teams and vendors to deliver clinical trials on time within budget and at the highest quality standards. Strategy & Execution: Shape study-level strategies and ensure alignment across global teams managing risks and driving solutions for operational challenges. Collaboration: Build strong partnerships with internal stakeholders and external collaborators to optimize study outcomes. Growth: Mentor team members support organizational initiatives and contribute to a culture of excellence. Lead and oversee multiple clinical trials from start-up to close-out. Develop and manage project plans budgets and resources. Ensure regulatory compliance and maintain high-quality data. Proactively identify and resolve risks to keep trials on track. Foster an inclusive collaborative and high-performing team environment. Bachelors degree (BA/BS) or equivalent in a relevant field. Therapeutic Area Experience: Oncology Neurology Immunology or similar is a plus Minimum 7 years experience in clinical operations and project management including multi-national trial leadership. Proven track record of leading complex global clinical trials and teams. Strong communication in English critical thinking and stakeholder engagement skills. Up to 25% travel may be required. Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned. Make a global impact grow your career and work with passionate professionals committed 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 shape 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. We kindly ask all applicants to send their CV in English. #LI-Hybrid If you come across a role that intrigues you but doesnt 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 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 . Visit 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: data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.Join Our Global Development Team!
Your Impact:What Youll Do:
What Were Looking For:
Why Join Us
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.
Required Experience:
Director
Key Skills
- Program assessment
- FDA Regulations
- Manufacturing & Controls
- Program Evaluation
- budget forecast
- Research Experience
- Operations Management
- Research & Development
- Strategic Planning
- Contract Management
- Leadership Experience
- negotiation
About Company
Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more
