Associate Director, Clinical Data Management

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. What if your next role helped change the course of a patient's life? At Bristol Myers Squibb, that's not a motivational tagline - it's the reality of what you'd be doing every single day. We're looking for an Associate Director of Clinical Data Management to join us at our Uxbridge site. This is a role where your expertise doesn't just support a clinical trial - it drives it. The data you champion, the standards you set, and the teams you lead are what ultimately move life-changing medicines from the lab to the people who need them most. If you're someone who finds purpose in precision, thrives in complexity, and wants to lead - not just participate - then read on. This is your chance to lead, not just deliver You'll step into a genuine leadership position at the heart of BMS's R&D pipeline — one of the most promising in the industry. You won't be managing data in isolation. You'll be the person that cross-functional teams turn to, the voice of data management in study teams and at the executive table, and the expert who sets the standard others follow. In practical terms, that means: * Owning end-to-end data management across one or more complex, high-stakes clinical development programmes — with the autonomy to shape how they run * Setting programme-level data standards in partnership with global teams, leaving a legacy that outlasts any single trial * Leading Data Quality Review meetings, ensuring the integrity and completeness of trial data that underpins regulatory submissions worldwide * Mentoring junior Data Management Leads, helping the next generation of talent grow — and growing your own leadership reputation in the process * Representing Data Management on cross-functional and regulatory submission teams, giving you visibility and influence across the full breadth of the organisation This isn't a role where you wait for direction. You are the direction. The problems you'll solve are genuinely hard and that's the point Clinical trials are complex. Multi-vendor. Multi-system. High-pressure. And the margin for error is slim when patient safety and regulatory approval are on the line. You'll be working with EDC systems (Medidata RAVE), integrating data from eCOA, External Data, and Safety Gateway platforms, and overseeing third-party vendors and CROs to ensure everything runs to the agreed SLA. You'll author and review critical study documentation — from Data Quality Management Plans to eCRF Completion Guidelines — and you'll lead or support Health Authority inspections and audits when it really counts. What does that mean for you? You'll build a track record that is visible, verifiable, and genuinely impressive. The kind of experience that doesn't just look good on a CV — it shapes who you are as a leader in this industry. You'll be part of something bigger than any single study BMS is a company that takes its mission seriously: to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. That mission runs through everything here, and in this role, you'll...