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Bei Bristol Myers Squibb lassen wir uns von einer einzigen Vision inspirieren - die Veränderung des Lebens von Patienten durch Wissenschaft. In den Bereichen Onkologie, Hämatologie, Immunologie und Herz-Kreislauf-Erkrankungen - und eine der vielfältigsten und vielversprechendsten Pipelines der Branche - trägt jeder unserer leidenschaftlichen Kollegen zu Innovationen bei, die bedeutende Veränderungen vorantreiben. Wir verleihen jeder Therapie, für die wir Pionierarbeit leisten, eine menschliche Note. Kommen Sie zu Bristol Myers Squibb  und machen Sie einen Unterschied. Location: Uxbridge Hybrid Working: 50% on site Are you ready to do the work of your career? At Bristol Myers Squibb, we believe that the right data, in the right hands, at the right time can change everything. Every clinical trial we run brings us closer to a treatment that could transform or save a patient's life. As our Senior Manager of Clinical Data Management,  you'll be the person who makes that possible. This isn't just a data role. It's a leadership position at the heart of our R&D pipeline; where your decisions, your standards, and your expertise directly shape the speed and quality of life-changing medicines reaching patients worldwide. What You'll Be Doing Leading Where It Matters Most You'll take the wheel on end-to-end clinical data management for some of our most complex and impactful trials. That means being the go-to person for both internal teams and external partners, the one who sets the bar for data quality and makes sure everyone clears it. • Drive data collection strategy across one or more complex clinical development projects, aligning cross-functional teams around clear, high-quality standards • Own the full data management lifecycle, from planning and collection through to clean, submission-ready datasets delivered on time • Shape the systems that power our trials, leading requirements gathering for EDC platforms and collaborating with partners across eCOA, External Data, and Safety Gateway • Chair Data Quality Review meetings to keep trial data current, complete, and audit-ready at every stage • Author and review key study documents, Data Quality Management Plans, Data Validation Plans, eCRF Completion Guidelines and more, ensuring consistency and compliance across the board Mentoring the Next Generation • One of the most rewarding parts of this role? You'll coach and guide junior Data Management Leads, helping them grow while raising the overall capability of the team. Your expertise becomes their foundation. Representing DM at the Highest Level • You'll sit at the table for cross-functional project teams and regulatory submission teams, and you'll be a key player during Health Authority inspections and audits. This is a role where your voice carries real weight. Vendor Oversight & Partnerships • Whether working with FSPs, CROs, or third-party vendors, you'll be the quality compass; monitoring deliverables, managing data currency throughout the trial, and holding partners accountable to SLAs that protect the integrity of our work. Driving Continuous Improvement • You'll contribute meaningfully to how we evolve as an organisation — supporting CAPA implementation and bringing fresh thinking to continuous improvement initiatives within Clinical Data Management. What's In It For You • Meaningful impact , your work directly supports the development of medicines that matter to millions of patients globally • Career elevation , step into a senior leadership role with visibility across R&D and a clear path toward Director-level progression • Cross-functional influence,  build relationships across clinical operations, regulatory, biostatistics, and beyond • Industry exposure , travel to conferences, investigator meetings, and regulatory engagements (approximately 5–10% travel) to stay at the forefront of your field • Intellectual challenge , work with cutting-edge data collection technologies and emerging industry trends that keep your skills sharp and future-proof What You'll Bring • A Bachelor's Degree (advanced degree preferred) and at least 5 years of relevant industry experience • A strong command of clinical drug development processes, FDA/ICH guidelines, and data management best practices • Hands-on experience with EDC systems; Medidata RAVE experience is a strong plus • Proven project management skills, with a PMP certification considered a bonus • The ability to translate complex data into clear insights through metrics analysis and reporting • Outstanding communication skills, whether you're presenting to senior leadership or collaborating with a vendor team, you know how to land the message • Familiarity with submission requirements including NDA, BLA, and MAA processes Ready to Apply? If you're someone who takes pride in doing rigorous work  and  inspiring others to do the same, someone who sees clinical data not just as numbers, but as the foundation of scientific truth, we'd love to hear from you. Join BMS. Transform patients' lives. Build your own. LI-Hybrid Wir setzen uns auf der ganzen Welt leidenschaftlich dafür ein, das Leben von Patienten mit schweren Krankheiten zu beeinflussen. Unsere gemeinsamen Werte Leidenschaft, Innovation, Dringlichkeit, Verantwortlichkeit, Inklusion und Integrität befähigen uns, unsere individuellen Talente und unterschiedlichen Perspektiven in einer integrativen Kultur einzusetzen und bringen das höchste Potenzial jedes unserer Kollegen hervor. Bristol Myers Squibb erkennt die Bedeutung von Ausgewogenheit und Flexibilität in unserer Arbeitsumgebung an. Wir bieten eine große Bandbreite wettbewerbsfähiger Leistungen, Dienste und Programme, die unseren Mitarbeitern die Ressourcen bereitstellen, ihre Ziele sowohl in der Arbeit als auch in ihrem Privatleben zu verfolgen. Unser Unternehmen verpflichtet sich dazu sicherzustellen, dass Menschen mit Behinderungen sich hervortun können. Dies erreichen wir durch einen transparenten Rekrutierungsprozess, angemessene Anpassungen des Arbeitsplatzes und laufende Unterstützung in ihren Rollen. Wenn Sie angemessene Anpassungen benötigen, um diese Bewerbung ausfüllen zu können, oder Fragen zu einem Teil des Rekrutierungsprozesses haben, richten Sie eine entsprechende Anfrage an [email protected]. Bewerber können die Genehmigung einer Anpassung beantragen, bevor sie ein Jobangebot annehmen. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [email protected] . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1603294 : Senior Manager, Clinical Data Management