IT Regulatory & Clinical Systems Leader – Radiopharma

Bristol-Myers Squibb Company

New Jersey

On-site

USD 166,000 - 221,000

Full time

4 days ago
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Benefits offered by this job

Health insurance
Flexible time off and holidays
Vacation benefits
Company-wide shutdown

Job summary

RayzeBio, a Bristol Myers Squibb company, seeks an Associate Director of IT Regulatory, Clinical and Enterprise Systems to lead digital solutions across Clinical Operations, Regulatory, Planning and Enterprise Systems. You will partner cross-functionally to enable growth, manage budgets, and drive a modern IT roadmap for radiopharmaceutical technologies.

Based in the US with on-site locations in Indianapolis or San Diego, you will guide regulatory inspection readiness, data integrity

Qualifications

  • 10+ years IT experience in a cGMP injectable or Radiopharmaceutical environment.
  • Proven technical leadership and management experience.
  • Demonstrated experience implementing automation and digitization projects.
  • BS/MS Information Technology or similar degree or equivalent experience

Responsibilities

  • Ensure Digital Roadmap is leveraged and aligned to business outcomes.
  • Lead a group of indirect reports and service providers.
  • Provide IT leadership to regulatory inspection readiness and data integrity initiatives.
  • Manage new demand and evolve digital solutions and mindset.
  • Identify key technology trends and how innovative technologies might be leveraged.
  • Participate in high-level strategic communications with business and leadership teams.
  • Develop long-term roadmaps (3 years) for capabilities with greatest impact.
  • Apply AI to improve team execution and decision-making.

Skills

Project leadership
Regulatory IT
Automation
Stakeholder influence
Budget management

Education

BS/MS Information Technology or similar

Tools

RIM
ERP systems

Job description

RayzeBio, a Bristol Myers Squibb company, seeks an Associate Director of IT Regulatory, Clinical and Enterprise Systems to lead digital solutions across Clinical Operations, Regulatory, Planning and Enterprise Systems. You will partner cross-functionally to enable growth, manage budgets, and drive a modern IT roadmap for radiopharmaceutical technologies.

Based in the US with on-site locations in Indianapolis or San Diego, you will guide regulatory inspection readiness, data integrity

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