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Associate Director, IT Regulatory, Clinical, and Enterprise Systems

Bristol-Myers Squibb

Software and Technology Jobs

Associate Director, IT Regulatory, Clinical, and Enterprise Systems

full-timePosted: Nov 7, 2025

Job Description

Accountable for continuous operation and maintenance of digital solutions for Clinical Operations, Regulatory, Supply chain planning and related Enterprise Systems. These systems include clinical site portal, RIM, supply chain planning, and other regulated functional solutions. Scope will also include associated infrastructure. Deliver on service level management scope and process with IT groups and/or vendor managed services, i.e., Service Level Agreements (SLA's), Disaster Recovery/Service Continuity, etc. Ensure Digital Roadmap leveraged and aligned to business outcomes. Drive for value realization. Lead a group of indirect reports and service providers to deliver effective, innovative and stable solutions that meet the needs of the organization. Active partner with the functional leaders. Collaborate with leadership to develop, support, and align strategies for business process improvements through information systems automation. Provide IT leadership to regulatory inspection readiness and data integrity initiatives. Ensure risk-based validation delivered for the functions. Manage new demand and evolve digital solutions and mindset Identify key technology trends and how innovative technologies might be leveraged to provide solutions to the organization. Participate in high-level strategic communications with the business and functional leadership teams Responsible for the development of long-term (3 year) roadmaps identifying capabilities that have the greatest impact on business capabilities for the organization. Partnering and benchmarking with external sources. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. 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 Strong project management skills with a proven track record of leading multi-disciplinary teams in a regulated environment. Ability to influence stakeholders at all levels and drive strategic initiatives. Leads complex, multi-disciplinary projects including resource and budget allocation and operational leadership. Oversees deliverable product, sets vision and standards for work products, challenges teams. It requires strong influence and trust, resilience in demanding situations, and the ability to encourage calm and rational behavior in teams. The leader identifies multiple solutions and recommendations for senior leaders, structures communications to achieve organizational goals, and tailors communication content and style for stakeholder understanding. The role also involves providing strategic feedback to vendors, synthesizing multiple analyses to solve broader business issues, and representing the discipline or function on program/project teams. Additionally, the leader identifies gaps in capabilities, ensures developmental opportunities for colleagues, sets direction with little guidance, contributes to multiple topic areas, and drives functional direction. Standard office environment coupled with GMP production and facility environment. Must be willing to wear personal protective equipment (PPE) as required. Must be comfortable working around radioactive materials. Periodic travel to other RayzeBio locations

About the Role/Company

  • Standard office environment coupled with GMP production and facility environment

Key Responsibilities

  • Accountable for continuous operation and maintenance of digital solutions for Clinical Operations, Regulatory, Supply chain planning, and related Enterprise Systems
  • Deliver on service level management scope and process with IT groups and/or vendor managed services, including Service Level Agreements (SLAs), Disaster Recovery/Service Continuity
  • Ensure Digital Roadmap is leveraged and aligned to business outcomes
  • Drive for value realization
  • Lead a group of indirect reports and service providers to deliver effective, innovative, and stable solutions
  • Active partner with functional leaders
  • Collaborate with leadership to develop, support, and align strategies for business process improvements through information systems automation
  • Provide IT leadership to regulatory inspection readiness and data integrity initiatives
  • Ensure risk-based validation is delivered for the functions
  • 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 the business and functional leadership teams
  • Responsible for the development of long-term (3 year) roadmaps identifying capabilities that have the greatest impact on business capabilities
  • Partnering and benchmarking with external sources
  • Leads complex, multi-disciplinary projects including resource and budget allocation and operational leadership
  • Oversees deliverable product, sets vision and standards for work products, challenges teams
  • Identifies multiple solutions and recommendations for senior leaders
  • Structures communications to achieve organizational goals and tailors communication content and style for stakeholder understanding
  • Provides strategic feedback to vendors
  • Synthesizes multiple analyses to solve broader business issues
  • Represents the discipline or function on program/project teams
  • Identifies gaps in capabilities
  • Ensures developmental opportunities for colleagues
  • Sets direction with little guidance
  • Contributes to multiple topic areas
  • Drives functional direction

Required Qualifications

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

Skills Required

  • Strong project management skills with a proven track record of leading multi-disciplinary teams in a regulated environment
  • Ability to influence stakeholders at all levels and drive strategic initiatives
  • Strong influence and trust
  • Resilience in demanding situations
  • Ability to encourage calm and rational behavior in teams

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Additional Requirements

  • Must be willing to wear personal protective equipment (PPE) as required
  • Must be comfortable working around radioactive materials
  • Periodic travel to other RayzeBio locations

Locations

  • Indianapolis RayzeBio, India
  • San Diego RayzeBio, Canada

Salary

Estimated Salary Rangemedium confidence

1,500,000 - 2,500,000 INR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strong project management skills with a proven track record of leading multi-disciplinary teams in a regulated environmentintermediate
  • Ability to influence stakeholders at all levels and drive strategic initiativesintermediate
  • Strong influence and trustintermediate
  • Resilience in demanding situationsintermediate
  • Ability to encourage calm and rational behavior in teamsintermediate

Required Qualifications

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

Responsibilities

  • Accountable for continuous operation and maintenance of digital solutions for Clinical Operations, Regulatory, Supply chain planning, and related Enterprise Systems
  • Deliver on service level management scope and process with IT groups and/or vendor managed services, including Service Level Agreements (SLAs), Disaster Recovery/Service Continuity
  • Ensure Digital Roadmap is leveraged and aligned to business outcomes
  • Drive for value realization
  • Lead a group of indirect reports and service providers to deliver effective, innovative, and stable solutions
  • Active partner with functional leaders
  • Collaborate with leadership to develop, support, and align strategies for business process improvements through information systems automation
  • Provide IT leadership to regulatory inspection readiness and data integrity initiatives
  • Ensure risk-based validation is delivered for the functions
  • 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 the business and functional leadership teams
  • Responsible for the development of long-term (3 year) roadmaps identifying capabilities that have the greatest impact on business capabilities
  • Partnering and benchmarking with external sources
  • Leads complex, multi-disciplinary projects including resource and budget allocation and operational leadership
  • Oversees deliverable product, sets vision and standards for work products, challenges teams
  • Identifies multiple solutions and recommendations for senior leaders
  • Structures communications to achieve organizational goals and tailors communication content and style for stakeholder understanding
  • Provides strategic feedback to vendors
  • Synthesizes multiple analyses to solve broader business issues
  • Represents the discipline or function on program/project teams
  • Identifies gaps in capabilities
  • Ensures developmental opportunities for colleagues
  • Sets direction with little guidance
  • Contributes to multiple topic areas
  • Drives functional direction

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

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Bristol-Myers Squibb logo

Associate Director, IT Regulatory, Clinical, and Enterprise Systems

Bristol-Myers Squibb

Software and Technology Jobs

Associate Director, IT Regulatory, Clinical, and Enterprise Systems

full-timePosted: Nov 7, 2025

Job Description

Accountable for continuous operation and maintenance of digital solutions for Clinical Operations, Regulatory, Supply chain planning and related Enterprise Systems. These systems include clinical site portal, RIM, supply chain planning, and other regulated functional solutions. Scope will also include associated infrastructure. Deliver on service level management scope and process with IT groups and/or vendor managed services, i.e., Service Level Agreements (SLA's), Disaster Recovery/Service Continuity, etc. Ensure Digital Roadmap leveraged and aligned to business outcomes. Drive for value realization. Lead a group of indirect reports and service providers to deliver effective, innovative and stable solutions that meet the needs of the organization. Active partner with the functional leaders. Collaborate with leadership to develop, support, and align strategies for business process improvements through information systems automation. Provide IT leadership to regulatory inspection readiness and data integrity initiatives. Ensure risk-based validation delivered for the functions. Manage new demand and evolve digital solutions and mindset Identify key technology trends and how innovative technologies might be leveraged to provide solutions to the organization. Participate in high-level strategic communications with the business and functional leadership teams Responsible for the development of long-term (3 year) roadmaps identifying capabilities that have the greatest impact on business capabilities for the organization. Partnering and benchmarking with external sources. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. 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 Strong project management skills with a proven track record of leading multi-disciplinary teams in a regulated environment. Ability to influence stakeholders at all levels and drive strategic initiatives. Leads complex, multi-disciplinary projects including resource and budget allocation and operational leadership. Oversees deliverable product, sets vision and standards for work products, challenges teams. It requires strong influence and trust, resilience in demanding situations, and the ability to encourage calm and rational behavior in teams. The leader identifies multiple solutions and recommendations for senior leaders, structures communications to achieve organizational goals, and tailors communication content and style for stakeholder understanding. The role also involves providing strategic feedback to vendors, synthesizing multiple analyses to solve broader business issues, and representing the discipline or function on program/project teams. Additionally, the leader identifies gaps in capabilities, ensures developmental opportunities for colleagues, sets direction with little guidance, contributes to multiple topic areas, and drives functional direction. Standard office environment coupled with GMP production and facility environment. Must be willing to wear personal protective equipment (PPE) as required. Must be comfortable working around radioactive materials. Periodic travel to other RayzeBio locations

About the Role/Company

  • Standard office environment coupled with GMP production and facility environment

Key Responsibilities

  • Accountable for continuous operation and maintenance of digital solutions for Clinical Operations, Regulatory, Supply chain planning, and related Enterprise Systems
  • Deliver on service level management scope and process with IT groups and/or vendor managed services, including Service Level Agreements (SLAs), Disaster Recovery/Service Continuity
  • Ensure Digital Roadmap is leveraged and aligned to business outcomes
  • Drive for value realization
  • Lead a group of indirect reports and service providers to deliver effective, innovative, and stable solutions
  • Active partner with functional leaders
  • Collaborate with leadership to develop, support, and align strategies for business process improvements through information systems automation
  • Provide IT leadership to regulatory inspection readiness and data integrity initiatives
  • Ensure risk-based validation is delivered for the functions
  • 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 the business and functional leadership teams
  • Responsible for the development of long-term (3 year) roadmaps identifying capabilities that have the greatest impact on business capabilities
  • Partnering and benchmarking with external sources
  • Leads complex, multi-disciplinary projects including resource and budget allocation and operational leadership
  • Oversees deliverable product, sets vision and standards for work products, challenges teams
  • Identifies multiple solutions and recommendations for senior leaders
  • Structures communications to achieve organizational goals and tailors communication content and style for stakeholder understanding
  • Provides strategic feedback to vendors
  • Synthesizes multiple analyses to solve broader business issues
  • Represents the discipline or function on program/project teams
  • Identifies gaps in capabilities
  • Ensures developmental opportunities for colleagues
  • Sets direction with little guidance
  • Contributes to multiple topic areas
  • Drives functional direction

Required Qualifications

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

Skills Required

  • Strong project management skills with a proven track record of leading multi-disciplinary teams in a regulated environment
  • Ability to influence stakeholders at all levels and drive strategic initiatives
  • Strong influence and trust
  • Resilience in demanding situations
  • Ability to encourage calm and rational behavior in teams

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Additional Requirements

  • Must be willing to wear personal protective equipment (PPE) as required
  • Must be comfortable working around radioactive materials
  • Periodic travel to other RayzeBio locations

Locations

  • Indianapolis RayzeBio, India
  • San Diego RayzeBio, Canada

Salary

Estimated Salary Rangemedium confidence

1,500,000 - 2,500,000 INR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strong project management skills with a proven track record of leading multi-disciplinary teams in a regulated environmentintermediate
  • Ability to influence stakeholders at all levels and drive strategic initiativesintermediate
  • Strong influence and trustintermediate
  • Resilience in demanding situationsintermediate
  • Ability to encourage calm and rational behavior in teamsintermediate

Required Qualifications

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

Responsibilities

  • Accountable for continuous operation and maintenance of digital solutions for Clinical Operations, Regulatory, Supply chain planning, and related Enterprise Systems
  • Deliver on service level management scope and process with IT groups and/or vendor managed services, including Service Level Agreements (SLAs), Disaster Recovery/Service Continuity
  • Ensure Digital Roadmap is leveraged and aligned to business outcomes
  • Drive for value realization
  • Lead a group of indirect reports and service providers to deliver effective, innovative, and stable solutions
  • Active partner with functional leaders
  • Collaborate with leadership to develop, support, and align strategies for business process improvements through information systems automation
  • Provide IT leadership to regulatory inspection readiness and data integrity initiatives
  • Ensure risk-based validation is delivered for the functions
  • 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 the business and functional leadership teams
  • Responsible for the development of long-term (3 year) roadmaps identifying capabilities that have the greatest impact on business capabilities
  • Partnering and benchmarking with external sources
  • Leads complex, multi-disciplinary projects including resource and budget allocation and operational leadership
  • Oversees deliverable product, sets vision and standards for work products, challenges teams
  • Identifies multiple solutions and recommendations for senior leaders
  • Structures communications to achieve organizational goals and tailors communication content and style for stakeholder understanding
  • Provides strategic feedback to vendors
  • Synthesizes multiple analyses to solve broader business issues
  • Represents the discipline or function on program/project teams
  • Identifies gaps in capabilities
  • Ensures developmental opportunities for colleagues
  • Sets direction with little guidance
  • Contributes to multiple topic areas
  • Drives functional direction

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

Target Your Resume for "Associate Director, IT Regulatory, Clinical, and Enterprise Systems" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Associate Director, IT Regulatory, Clinical, and Enterprise Systems. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Associate Director, IT Regulatory, Clinical, and Enterprise Systems" , Bristol-Myers Squibb

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

Answer 10 quick questions to check your fit for Associate Director, IT Regulatory, Clinical, and Enterprise Systems @ Bristol-Myers Squibb.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.