Sr. Manager, RIM Systems and Publishing

Essential duties and responsibilities include the following. Other duties may be assigned.

- Serve as a business administrator and business owner for Veeva Vault RIM platforms (Submissions, Submissions Archive, and Publishing). - Lead Veeva Vault RIM governance, optimization, end-user support, and continuous improvement of Regulatory Operations processes through effective use of Veeva Vault RIM. - Maintain and govern RIM master data, metadata standards, controlled vocabularies, relationships, and business rules to ensure data integrity, consistency, traceability, reporting accuracy, publishing readiness, and inspection readiness. - Lead Vault Publishing administration and assist with validation and implementation. - Support submission leads with content plan development, publishing configuration, workflows, publishing rules, validation, troubleshooting, and submission readiness activities - Develop and deliver system training, SOPs, work instructions, job aids, process flows, and governance documentation. - Partner with IT and Quality, as applicable, to support release management, system validation, change control, user access management, and compliance requirements. - Develop and maintain system metrics, dashboards, and reports to support operational oversight, compliance monitoring, data quality, and leadership decision-making.

- Maintain current knowledge of Veeva Vault RIM functionality, regulatory submission requirements, electronic publishing standards, and industry best practices. - Perform and/or support submission publishing activities as needed to support business priorities and resource demands.

- Bachelor's degree with 8+ years of relevant experience in regulatory systems or regulatory operations.

- Hands-on experience administering and supporting Veeva Vault RIM applications, including Submissions, Submissions Archive, and Publishing - Experience with eCTD publishing solutions and regulatory submission workflows. - Experience supporting Veeva RIM Publishing implementation preferred.

- Strong understanding of regulatory submission processes, eCTD structure, publishing requirements, and submission lifecycle management. - Strong understanding of data governance, metadata management, document classification, and inspection readiness principles. - Ability to translate business requirements into practical system processes and governance standards. - Strong troubleshooting skills for complex system, publishing, and process issues. - Ability to train and support end users with varying levels of system experience. - Highly organized, with the ability to manage system initiatives, governance activities, user support, and operational priorities. - Ability to collaborate effectively with Regulatory Affairs, IT, Quality, vendors, and cross-functional business users. - Proactive, professional, and confident.

While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 15 pounds. Specific vision abilities required by this job include close vision and distance vision.

RayzeBio was acquired by Bristol Myers Squibb (BMS) in 2024 and is a wholly-owned subsidiary of BMS; however, RayzeBio will continue to operate as a standalone organization.

BMS and RayzeBio are dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com .

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BMS and RayzeBio will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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