At a Glance
- Tasks: Lead AI-powered safety operations and transform global safety data into smarter outcomes.
- Company: Join a leading biopharma company committed to patient safety and innovation.
- Benefits: Competitive salary, diverse team, and opportunities for professional growth.
- Other info: Work in a dynamic, multicultural environment with a focus on continuous improvement.
- Why this job: Drive real change in patient safety with cutting-edge technology and a global impact.
- Qualifications: 10+ years in Pharmacovigilance with strong leadership and AI experience.
The predicted salary is between 100000 - 150000 £ per year.
As Director of Digitized Case Processing & Device Vigilance, you’ll architect the next generation of AI‑powered safety operations at one of the world’s leading biopharma companies, turning complex global safety data into faster, smarter and more compliant outcomes. Leading a globally distributed team across the US, UK, and India, you’ll sit at the intersection of cutting‑edge technology and patient safety — driving real change that matters.
What You’ll Own
- AI & Digital Transformation
- Design and deliver BMS’s multi‑year roadmap for intelligent ICSR case processing using AI, NLP, RPA, OCR, and LLMs
- Deploy and validate next‑generation platforms (ArisGlobal LifeSphere, IQVIA Vigilance Detect, Oracle Argus AI workflows) in a fully GxP‑compliant environment
- Govern a human‑in‑the‑loop (HITL) oversight framework ensuring AI‑assisted decisions meet global regulatory standards
- Champion ICH E2B(R3) digital submission standards across all BMS reporting pathways
- Device Safety & MDR Compliance
- Own BMS’s global Medical Device Reporting obligations (21 CFR Part 803), including timely 5‑day and 30‑day eMDR FDA submissions
- Lead EU MDR/IVDR device vigilance integration and EudraVigilance reporting under GVP Module VI
- Define combination product dual‑reporting workflows across jurisdictions, partnering with Regulatory Affairs, Device Development, and Medical Affairs
- Global Leadership & Governance
- Lead a high‑performing, multicultural team across the US, UK, and India within a matrix organisation spanning Japan and Switzerland
- Drive cross‑functional governance with Safety, IT, Quality, Legal/Privacy, and Regulatory stakeholders
- Represent Case Management in enterprise‑wide digital programs, system upgrades, and agency interactions
- Quality, Compliance & Continuous Improvement
- Ensure inspection‑ready compliance with ICH E2A/E2B(R3), GVP Modules VI & VII, 21 CFR Parts 314/600/803, EU MDR 2017/745, GDPR, HIPAA, and EMA AI pharmacovigilance strategy
- Build a KPI framework tracking ICSR cycle times, automation accuracy, ingestion rates, and MDR compliance
- Embed a lean, right‑first‑time culture with root cause analysis and continuous improvement at its core
What You Bring
- 10+ years in Pharmacovigilance or Drug Safety, with 3–5 years at Director level or equivalent
- 7+ years of hands‑on ICSR case processing in pharma, biotech, or CRO settings
- Proven track record deploying AI/NLP/RPA/ML solutions in a regulated GxP environment
- Direct experience with MDR reporting (21 CFR Part 803), EU MDR/IVDR, and combination product workflows
- Familiarity with Oracle Argus, Veeva Vault Safety, or ArisGlobal LifeSphere, and electronic submission platforms (FAERS, EudraVigilance, MHRA Yellow Card)
- Experience leading regulatory inspections (FDA, EMA, MHRA or equivalent)
Leadership
- Demonstrated ability to lead and develop geographically dispersed, multicultural teams
- Strong vendor and BPO management experience in outsourced case processing
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, Biomedical Engineering, Computer Science, or related field (required)
- Advanced degree (Master’s, PharmD, MD, or PhD) (preferred)
- Qualifications in Digital Health, Data Science, AI/ML, or Health Informatics (highly desirable)
Director, Digitized Case Processing & Device Vigilance in Uxbridge employer: Bristol Myers Squibb EU Policy
At Bristol Myers Squibb, we pride ourselves on being a leading biopharma company that fosters a culture of innovation and collaboration. As a Director in Digitized Case Processing & Device Vigilance, you will not only have the opportunity to lead a diverse, global team but also drive meaningful advancements in patient safety through cutting-edge technology. Our commitment to employee growth, inclusive work environment, and dedication to compliance ensures that you will thrive in your role while making a significant impact on healthcare outcomes.
Contact Details:
Bristol Myers Squibb EU Policy Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Director, Digitized Case Processing & Device Vigilance in Uxbridge
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We think you need these skills to ace Director, Digitized Case Processing & Device Vigilance in Uxbridge
Some tips for your application 🫡
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How to prepare for a job interview at Bristol Myers Squibb EU Policy
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Bristol Myers Squibb EU Policy that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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