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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. The Clinical Trial Physician serves as a primary source of medical accountability and oversight for multiple clinical trials, and manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities. It has matrix management responsibilities across the internal and external network and the role provides medical and scientific expertise to cross-functional BMS colleagues. Position responsibilities Medical Monitoring: • Team Leadership & Collaboration  — Serve as a key contributor to the Study Delivery Team (SDT) and Clinical Development Team (CDT), partnering with Clinical Scientists to provide medical oversight on protocol development, including inclusion/exclusion criteria and safety considerations • Medical Monitoring & Safety  — Lead medical and eligibility data reviews, assess safety-related serious adverse events in partnership with Worldwide Patient Safety, and oversee site interactions and safety narratives • GCP & Compliance  — Uphold all GCP obligations for clinical conduct, safety management guidelines, and maintain up-to-date required training Clinical Development Expertise & Strategy: • Clinical Strategy & Protocol Design  — Collaborate with the Clinical Development Lead to design and develop clinical plans and protocols, with a strategic focus on drug/asset knowledge, disease area science, and regulatory targets • Medical Oversight & Accountability  — Provide medical accountability across a group of studies, leading benefit/risk analyses within a matrix team environment alongside Clinical Scientists • Study Execution & Delivery  — Partner with Clinical Scientists to support all aspects of study delivery, including site activation, enrollment, and adjudication of protocol violations and deviations • Stakeholder Engagement & Thought Leadership  — Build and maintain relationships with principal investigators and key opinion leaders to inform emerging science, biomarker research, and clinical program design • Scientific Expertise & Education  — Maintain deep, up-to-date knowledge of the disease area through conference attendance and literature review, while staying informed on the competitive landscape and providing ongoing protocol-specific medical education to study teams and investigators Health Authority Interactions & Publications: • Health Authority & Advisory Engagement  — Serve as the medical point of expertise in key Health Authority interactions and advisory board meetings • Regulatory Writing & Submissions  — Author and draft clinical content for CSRs, regulatory reports, briefing books, and submission documents, including clinical narratives, in partnership with Clinical Scientists Qualifications and experience • MD required (or equivalent) • 5 or more years of Industry experience and/or clinical trials experience is required • Ability to communicate information clearly and lead presentations in scientific and clinical settings • Subspecialty training in applicable therapeutic area desired • Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation • Expertise in drug development process • Expertise in the components needed to execute an effective clinical plan and protocols • Strong leadership skills with proven ability to lead and work effectively in a team environment • Domestic and International travel may be required. 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. R1604606 : Director, Global Clinical Physician-Immunology