Trial Manager, Late Development

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 operational execution of Late Development Book of Work across various therapeutic areas and study types (e.g., NIR, ISR, PAA, Phase IV). Act as point of contact for external study sponsors and internal stakeholders. 

Duties/Responsibilities

• Manages protocols within a complex matrix environment for successful and timely operational execution of research from start to end
• Focused on project management concepts to support management of issues, risks, timelines, and budget
• Leverages interpersonal and influencing skills to foster partnerships across multidisciplinary teams

BMS-Sponsored Studies

• Monitor trial progress and study budget
• Lead study team meetings
• Address and manage obstacles
• Identify issues and risks, escalating appropriately
• Oversee vendors
• Manage and comply with various quality and compliance systems

Non-BMS Sponsored Studies

• Lead operational start-up, maintenance, and close-out 
• Serve as primary point of contact for study Sponsor  
• Liaise with Medical and global stakeholders to monitor study progress and ensure data deliverables are met  

Qualifications

Experience Requirements

• 2-4 years of demonstrated project management experience of which at least one should have been in the pharmaceutical or healthcare industry
• Experience in execution of clinical trials demonstrating project management and organizational skills

Understanding of GCP, ICH Guidelines, and Country regulatory environment

• Knowledge and understanding of clinical research processes, regulations, and methodology 
• Have planning skills and independent decision-making ability
• Organizational and time management skills; ability to effectively manage multiple competing priorities and influence cross-functionally
• Ability to think critically, identify, and neutralize risks
• Good verbal and written communication skills (both in English and Japanese)
• Microsoft Suite
• Able to work with Clinical Trial Management Systems (CTMS)

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.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. 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.

R1602943 : Trial Manager, Late Development