Director, Veeva Clinical CTMS Lead
Pfizer
11 days ago
Remote friendly (Bothell, WA)
United States
Operations
Role Summary
Lead drug development process and change management/support for the Clinical Data & Information Sciences (CD&IS) / Clinical Development & Operations (CD&O) system portfolio, partnering to ensure timely data integrity and compliance.
Responsibilities
- Integrate CD&IS solutions into business processes; define strategies/best practices for content management systems.
- Drive continuous improvement of scalable solutions; implement infrastructure updates to enhance end-user experience.
- Ensure critical information/records in CD&O repositories are compliant, protected, retained per schedules, and available for business needs.
- Participate in governance, change management, roadmap, and budget planning.
- Lead CD&IS teams; gather/define business requirements and improve business/support processes.
- Resolve complex operational issues and influence stakeholder decisions.
- Coordinate system release activities; interface with strategic projects and vendors to influence usability/features/performance.
- Develop test strategies and user acceptance testing approaches for releases.
- Serve as SME/content interface for regulators; provide inspection readiness consultation and in-room support during inspections/audits.
Required Qualifications
- BS + 8 yrs (or MBA/MS + 7; PhD/JD + 5; MD/DVM + 4)
- Knowledge of healthcare/pharma drug development regulations and Clinical Trial processes (startup, site management/monitoring, operational reporting)
- Cross-functional collaboration, strong communication/presentation, project management/organization, analytical/problem-solving.
Preferred Qualifications
- MS with relevant pharma industry experience; leading cross-functional teams/large projects
- Advanced Veeva Clinical/other CTMS; strong compliance/regulatory knowledge
- Digital transformation leadership; fast-paced multitasking; AI tools experience (e.g., ChatGPT/Copilot).
Work/Other
- Operations focus; may require unplanned nights/weekends.
- Hybrid: live within commuting distance; ~2.5 days/week on-site.
- Apply by: June 10, 2026.
Lead drug development process and change management/support for the Clinical Data & Information Sciences (CD&IS) / Clinical Development & Operations (CD&O) system portfolio, partnering to ensure timely data integrity and compliance.
Responsibilities
- Integrate CD&IS solutions into business processes; define strategies/best practices for content management systems.
- Drive continuous improvement of scalable solutions; implement infrastructure updates to enhance end-user experience.
- Ensure critical information/records in CD&O repositories are compliant, protected, retained per schedules, and available for business needs.
- Participate in governance, change management, roadmap, and budget planning.
- Lead CD&IS teams; gather/define business requirements and improve business/support processes.
- Resolve complex operational issues and influence stakeholder decisions.
- Coordinate system release activities; interface with strategic projects and vendors to influence usability/features/performance.
- Develop test strategies and user acceptance testing approaches for releases.
- Serve as SME/content interface for regulators; provide inspection readiness consultation and in-room support during inspections/audits.
Required Qualifications
- BS + 8 yrs (or MBA/MS + 7; PhD/JD + 5; MD/DVM + 4)
- Knowledge of healthcare/pharma drug development regulations and Clinical Trial processes (startup, site management/monitoring, operational reporting)
- Cross-functional collaboration, strong communication/presentation, project management/organization, analytical/problem-solving.
Preferred Qualifications
- MS with relevant pharma industry experience; leading cross-functional teams/large projects
- Advanced Veeva Clinical/other CTMS; strong compliance/regulatory knowledge
- Digital transformation leadership; fast-paced multitasking; AI tools experience (e.g., ChatGPT/Copilot).
Work/Other
- Operations focus; may require unplanned nights/weekends.
- Hybrid: live within commuting distance; ~2.5 days/week on-site.
- Apply by: June 10, 2026.