Global Trial Management - Resourcing Lead

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.

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

Position Summary

• Responsible for strategic planning, allocation and optimization of Global Trial Leads (GTL) within the Global Trial Management department. This role may also support resourcing of Global Trial Associates (GTAs).

• This role ensures that appropriately skilled staff are aligned to business priorities, enabling timely and efficient delivery of clinical trials.

• Leverage data-driven resource management across programs, improving visibility, utilization and cost efficiency in a complex, matrixed global environment.

• Conduct quarterly review of the book of work (BoW) to assess gaps, surpluses and risks in capacity for GTL and GTAs to support headcount planning and hiring decision making.

• Consistently solicit line manager feedback to understand state of GTL performance and capacity.

• Facilitate GTL assignment approval process; ensure Operation Portfolio Leads (OPLs), Therapeutic Area (TA)/Pillar Heads are aligned with assignments.

• Collaborate with resource management team on resourcing algorithm for GTL role.

Key Responsibilities

• Assign resources across studies based on priority, skillset and capacity.

• Optimize utilization while supporting employee development and engagement

• Track and adjust allocations dynamically as study needs evolve

• Stakeholder management: Must balance interests of TA heads with ensuring full execution of the BoW

• Initiative/proactiveness: Must continually review resource demand, anticipate future shortages, & flag to leadership early to prevent negative impacts

• Organization/attention to detail: Must be able to collect/collate data from multiple stakeholders / sources to understand resourcing trends

• Analytics with action: Utilize data analysis and reporting tools to track resource utilization, identify trends, and provide insights to stakeholders for decision-making.

• Drive continuous improvement in resource planning processes and tools

 

Qualifications & Experience

• BA/BS or equivalent degree; Advanced degree preferred

• Minimum 8 years’ experience in resource management or management experience with resourcing accountability within the pharmaceutical industry

• Familiarity with FTE-to-headcount conversations

• Prior experience in clinical trials operations with demonstrated focus on enterprise performance to bring value and efficiency to an organization.

• Strong proficiency in resource management tools, such as Microsoft Excel for data manipulations, and potentially specialized software like Planisware for planning and forecasting.

• Strong communication (both verbal and written), interpersonal, and organizational skill are crucial for collaborating with various stakeholders and presenting complex data

• Ability to prioritize tasks, multi-task, and work independently in a fast-paced environment.

• A collaborative mindset and ability to build partnerships and work effectively in a team-oriented setting.
• Strong leadership skills, self-motivation, and the ability to adapt to changing priorities.

 

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 [email protected]. 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.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [email protected]. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1603688 : Global Trial Management - Resourcing Lead