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 rich in diversity. 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:

Accountable for implementing and supporting strategic information systems that enable Global Development Operations (GDO) function, specifically focusing on Veeva Clinical Vault (Veeva CTMS, Veeva eTMF). This role owns end-to-end responsibility for managing the build and run of GDD technology assets, ensuring they are reliable, accessible, & secure.

Specific responsibilities:

• Partner with IT Product Managers to plan, prioritize, deliver & support strategic digital capabilities and ensure maximum value is achieved.

• Identify, design, and develop technical solutions to meet business demand.

• Manage the build and run of technology assets.

• Manage Total Cost of Ownership (build & run) and the key drivers behind them to ensure the digital capabilities are cost efficient.

• Influence vendor roadmaps to align with BMS strategy.

Requirements:

• Must have 10+ years of related work experience in a Biopharmaceutical environment.

• BS/BA in Engineering, Computer Science or Life Sciences (or other quantitative related discipline). Graduate Degree or higher-level education preferred.

• Must have Veeva Clinical Vault expertise, with specific knowledge of Veeva CTMS and eTMF.

• Must have broad technology expertise, strong working knowledge of Pharmaceutical R&D business processes, particularly in Clinical Trial Operations, with demonstrated command of key concepts, systems and processes.

• Preferred - certified in Veeva Vault Administration

• Should have a demonstrated track record in implementing complex technical solutions, developing software applications following structured SDLC processes in a regulated (GxP) environment and leading technical teams.

• Demonstrated competency in execution of multiple large projects simultaneously within a Product Model leveraging Agile methods, from concept initiation through delivery and steady-state operations.

• Experience working with offshore software development models is preferred.

• Critical thinking in dealing with complex technical issues and working with key business stakeholders to develop solutions for short-term remediation and long-term strategy.

• Experience in evaluating new technologies, delivery methods (e.g., SaaS/PaaS/IaaS), and services, and influencing the negotiation process for vendor products.

• Must possess excellent written and verbal skills and demonstrate an ability to effectively communicate at all levels of the organization including executive stakeholders.

• Ability to achieve successful consensus among differing priorities and stakeholders in both the IT and Business communities.

• Must be a relationship builder and capable of working effectively in a highly matrix organization with strong communication, planning, and collaboration skills.

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 an inclusive culture, promoting diversity 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 a diverse 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 adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility 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: https://careers.bms.com/california-residents/

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Company: Bristol-Myers Squibb

Req Number: R1584995

Updated: 2024-09-15 02:43:01.555 UTC

Location: Princeton-NJ

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.