Senior Counsel, Regulatory Law
Bristol Myers SquibbAbout the role
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.
Summary:
This role will have responsibility for providing Legal support to different stakeholders within Global Medical, Global Commercialization Excellence and Business Insights and Technology. The person in the role will be required to establish professional credibility and relationships with executive level commercialization colleagues and work effectively across a wide array of issues and stakeholders independently and in collaboration with Law Department colleagues.
Responsibilities:
Anticipate and proactively identify legal issues and provide clear, operational and effective legal advice that supports informed decisions and applies an enterprise view
Collaborate across the Law Department matrix to ensure delivery of seamless, comprehensive legal advice.
Deliver effective presentations to Law Department and Business Units.
Lead and organize functional or substantive working groups assessing significant legal issues.
Leverage knowledge of emerging legal and industry issues and trends to inform advice and address potential legal risk.
Lead simplification of policies, procedures and guidance affecting business activities.
Required Qualifications and Desired Experience:
Education: A law degree from a US Law School.
Knowledge: Broad knowledge of healthcare law, including advertising and promotion, anti-kickback and bribery laws, regulatory policy, and contracts.
Experience: At least five to eight years of legal, regulatory and/or compliance experience, preferably with a law firm that advises companies in highly regulated industries or in-house at a pharmaceutical or biotech or medical device company. Successful experience in cross-functional interactions is required.
Skills: Demonstrated ability to establish and maintain strong relationships across the business and within the Law Department. Ability to prioritize and manage multiple projects under deadline pressure. Flexibility to work on a broad range of matters. Ability to communicate complex issues clearly, verbally and in writing.
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
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