At a Glance
- Tasks: Lead AI-powered safety operations and manage a diverse global team.
- Company: Bristol Myers Squibb, a leader in biopharma innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Join a dynamic team making a real impact in the biopharma sector.
- Why this job: Transform complex safety data into compliant outcomes and drive innovation.
- Qualifications: 10+ years in Pharmacovigilance with experience in ICSR case processing.
The predicted salary is between 80000 - 120000 £ per year.
Bristol Myers Squibb EU Policy is seeking a Director of Digitized Case Processing & Device Vigilance to lead AI-powered safety operations, transforming complex safety data into compliant outcomes. The role entails managing a diverse team across the US, UK, and India while ensuring regulatory compliance in the biopharma sector.
The ideal candidate should have over 10 years in Pharmacovigilance, with proven experience in ICSR case processing and deploying innovative AI solutions within regulatory frameworks.
Global Director, AI-Powered Safety & Device Vigilance in Uxbridge employer: Bristol Myers Squibb EU Policy
Bristol Myers Squibb is an exceptional employer that champions innovation and collaboration in the biopharma sector. With a strong commitment to employee growth, we offer extensive training and development opportunities, fostering a culture of inclusivity and teamwork across our global teams in the US, UK, and India. Our focus on AI-powered solutions not only enhances compliance but also empowers our employees to make a meaningful impact in patient safety and care.
Contact Details:
Bristol Myers Squibb EU Policy Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Global Director, AI-Powered Safety & Device Vigilance in Uxbridge
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We think you need these skills to ace Global Director, AI-Powered Safety & Device Vigilance in Uxbridge
Some tips for your application 🫡
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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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