Bristol Myers Squibb
Director,DigitizedCaseProcessing&DigitalAdverseEventInterfaces
Neural analysis suggests this role is
optimal for Director candidates.
“Director, Digitized Case Processing & Digital Adverse Event Interfaces at Bristol Myers Squibb. Skills: Digitized Case Processing, Digital Adverse Event Interfaces, AI/NLP, Pharmacovigilance. Lead AI-powered transformation of adverse event intake. Define and own digital intake roadmap”
What You'll Achieve.
Genuinely automated, touchless AE case creation workflows; Validated, auditable data pipelines; Programme is always audit-ready; Touchless processing rates; Intake cycle times; Data completeness; Literature screening accuracy; Vendor SLA performance
Industry & Context.
Identify bottlenecks; Continuously raise the bar
Travel to visit customers, patients or business partners, Attend meetings on behalf of BMS
What They're Looking For.
Must Have
10+ years in Pharmacovigilance or Drug Safety, 3–5 years at Director level, 7 years of hands-on experience in ICSR data acquisition, case intake, or processing in pharma, biotech, or CRO environments, Ability to take a digital transformation vision and make it real, Translating ambiguous future-state thinking into clear, actionable roadmaps that get delivered, Comfortable in a regulatory conversation about ICH E2B(R3) compliance, Comfortable in a technical deep-dive on AI/NLP classifier performance, Experience during FDA, EMA, MHRA, and PMDA inspections
Nice to Have
Experience deploying AI, NLP, OCR, or RPA in a GxP-regulated environment, Proven track record building AE data interfaces with internal and external partners, Literature screening programme management, including AI-assisted platforms, Deep knowledge of ICH E2B(R3) across at least two major ICH regions, Familiarity with ARIS Global LifeSphere, Oracle Argus, or Veeva Vault Safety, Experience managing cross-regional teams, Exposure to AI governance in life sciences
What You'll Do.
Lead AI-powered transformation of adverse event intake
Define and own digital intake roadmap
touchless AE case creation workflows
Own interfaces connecting safety ecosystem
Drive ICH E2B(R3) adoption
Replace manual transmissions with data pipelines
Lead digital transformation of literature screening
Move to AI/NLP-driven screening
Govern search string development
Manage AI classifier calibration
Build and lead global team
Define career pathways
Upskill team in AI/ML fundamentals
Develop next generation PV leaders
Design and own KPI framework
Use operational analytics and dashboards
How You'll Work.
Team & Collaboration
Cross-functional coordination; Vendor/stakeholder management; Manage vendors; Build interfaces that work; Manage cross-regional teams; Collaborate with product teams; Work with licensing partners; Work with regulatory portals
Communication Scope
Regulatory conversation; Technical deep-dive
Process & Methodology
Develop actionable roadmaps, Programme management
Full Job Description
**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](https://careers.bms.com/working-with-us). **What if your next role actually mattered - not just to your career, but to patients around the world?** At Bristol Myers Squibb, we believe that getting patient safety information right - faster, smarter, and more reliably, isn't just an operational goal. It's a moral one. Every adverse event we capture more accurately, every process we automate with precision, every AI model we govern responsibly: it all traces back to a real person whose safety depends on us getting it right. That's the weight and the privilege of this role. And if that excites rather than intimidates you, read on. **What are we actually looking for?** **We 're looking for a Director of Digitized Case Processing & Digital Adverse Event Interfaces** \- a leader who sits comfortably at the crossroads of pharmacovigilance science, cutting-edge technology, global regulation, and people leadership. You're probably already senior in your PV career. You've led teams, managed vendors, survived inspections, and built interfaces that actually work. But you're res
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