Manager, Patient Safety, Epidemiology Science and Execution

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Have you ever wondered what happens after a medicine reaches a patient? Behind every approved therapy, there's a team asking the hard questions —  Is it safe? For whom? Under what conditions?  At Bristol Myers Squibb, that team is us. And we're looking for someone like you to help answer them. Your Work Will Reach Further Than You Think As a Manager in Patient Safety / Epidemiology Science and Execution , you won't just be pushing papers or ticking compliance boxes. You'll be part of the scientific machinery that ensures BMS medicines are as safe as they are transformative. Think about it: the data you analyze, the protocols you help draft, the literature you review — these feed directly into benefit-risk decisions that shape how doctors prescribe, how regulators approve, and ultimately, how patients live. That's not abstract. That's real impact . What You'll Actually Be Doing You'll work within a collaborative, senior-led epidemiology team, which means you'll be supported and mentored but you'll also be genuinely  trusted  with meaningful work from day one: Own your deliverables  - You'll be accountable for executing assigned epidemiology study components, from literature reviews and data source assessments to contributing directly to study protocols, analysis plans, and regulatory documents. Your fingerprints will be on science that matters. Contribute to regulatory-grade science  - You'll draft sections of safety study protocols and study reports, risk management plans, aggregate safety reports,  learning firsthand how rigorous, audit-ready science is built. If you've ever wanted to understand how pharma regulatory submissions come together, you're about to find out . Work across the organisation  - You'll coordinate with cross-functional teams, manage timelines, and navigate dependencies. You'll grow your stakeholder management skills in an environment where collaboration is the norm, not the exception. Spot problems before they become problems  - By identifying execution-level risks and escalating with proposed solutions, you'll quickly develop a professional instinct that's invaluable in any scientific career. Help shape how we work - You'll actively contribute to continuous improvement initiatives, meaning your ideas about quality and efficiency won't disappear into a suggestion box, they'll be heard. What You'll Gain (Beyond the Job Title) Execute post marketing safety study components - A portfolio of real-world evidence work in a globally recognised pharma company Draft regulatory documents - Deep expertise in the language and standards of international drug regulation Work with senior epidemiologists - A mentorship network and scientific foundation you can't get from a textbook Coordinate cross-functional activities - Project management skills that travel with you across your entire career Support inspection-ready documentation - A reputation for quality and precision, the gold standard in science Contribute to CI initiatives - A voice in how science gets done at BMS You Might Be Exactly Who We're Looking For If… You have a  scientific or biomedical degree  - whether that's a BS, MPH, PharmD, RN, MD, PhD or equivalent and at least 2 years of relevant experience (yes, that can include hands-on work from your training). You're the kind of person who: Reads the details others miss Juggles multiple priorities without dropping the scientific thread