Clinical Systems Analyst

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: us as a Clinical Systems Senior Analyst and make a meaningful impact on clinical research!

In this dynamic role youll champion innovation and continuous improvementsupporting clinical study teams streamlining protocols managing essential documentation and orchestrating collaborative workshops.

Youll operate with autonomy and build collaborative partnerships across functions ensuring consistently high-quality outcomes while upholding our commitment to integrity innovation and inclusion.

Key Responsibilities

• Executes the protocol simplification objectives across multiple therapeutic areas.
• Sets priorities for the team to ensure task completion and connectivity to clinical protocol process.
• Drive process improvements and technology enhancements in partnership with IT and other teams.
• Ensure alignment of clinical study design with quality-by-design principles.
• Build and maintain a digital document management system for accurate logging tracking and secure archiving of workshop materials.
• Lead workshops and guide teams in using supporting platforms effectively.
• Operate independently while fostering collaboration in a matrixed environment.
• Develop key performance indicators (KPIs) to measure protocol simplification success.
• Monitor analyze and report on metrics such as review turnaround times and workload distribution.
• Lead road-shows and training sessions to ensure consistent messaging and adoption.
• Provide timely updates and status reports to management.
• Prepare and distribute training materials guidance documents and stakeholder communications.
• Support audit and inspection readiness through document retrieval and coordination.

Required Education & Experience

• Bachelors degree in life sciences healthcare business administration or related field
• 3-5 years (minimum) of experience in clinical research biopharma or a regulated industry

Required Skills Competence and Knowledge

• Conceptual and practical expertise in own discipline and basic knowledge of related disciplines
• Innovative mindset with a passion for leveraging technology to improve processes
• Proven commitment to quality compliance and continuous improvement
• Strong organizational and time management skills with attention to detail
• Proficiency with Microsoft Office document management systems AI and other data analytic tools
• Demonstrated commitment to quality compliance and process improvement
• Ability to work collaboratively and adapt in a fast-paced environment

#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
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 . Visit 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: Protection

We will never request payments financial information or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.