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Job Description
📋 Description
- Lead complex RA submission projects with cross-functional teams.
- Maintain submission content planners and timelines.
- Interface with publishing vendors and internal teams.
- Provide guidance on submission processes and specs.
- Coordinate publishing and ensure regulatory compliance.
- Mentor staff and drive process improvements.
🎯 Requirements
- Bachelor’s degree required.
- 6 years pharma or related experience with publishing tools.
- Experience with Documentum, eCTDXPress/ISIPublisher, ISI Toolbox/DocuBridge/Insight, Adobe Acrobat.
- Regulatory Affairs experience preferred; QA/R&D/support acceptable.
- Proven leadership and project management skills.
🎁 Benefits
- Competitive compensation package.
- Medical/dental/vision insurance.
- 401(k) plan and long-term incentives.