$149,860 – $181,595
Listed on Bristol Myers Squibb’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role manages Veeva Vault regulatory information management systems and publishing workflows for a biotech company, serving as both technical administrator and business owner for submission platforms. It suits experienced regulatory operations professionals who combine deep domain knowledge of submission processes with hands-on system administration and can lead governance, user support, and continuous improvement across complex platforms.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's degree
- 8+ years regulatory systems or operations experience
- Hands-on Veeva Vault RIM administration (Submissions, Archive, Publishing)
- eCTD publishing solutions experience
- Regulatory submission workflows knowledge
- Data governance and metadata management understanding
- Ability to translate business requirements into system processes
- Complex troubleshooting skills
- End-user training capability
- Cross-functional collaboration skills
Nice to have
- Veeva RIM Publishing implementation experience