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Veeva Vault Administrator Jobs (NOW HIRING)

$91K - $122K/yr

Serve as Veeva Vault RIM Business Administrator in coordination with IT * Provide user support, training, and change management * Partner with regional RA teams to identify and implement system ...

NY · On-site

$91K - $122K/yr

Serve as Veeva Vault RIM Business Administrator in coordination with IT * Provide user support, training, and change management * Partner with regional RA teams to identify and implement system ...

Support integration between Veeva Vault Clinical and other clinical systems, including EDC platforms and CRO partner systems, and collaborate with Veeva Administrators on system configuration ...

Salesforce certifications, such as Administrator, Platform Developer, or Salesforce Life Sciences Cloud credentials. * Veeva Vault certifications or prior hands-on experience with Veeva CRM or Vault ...

Salesforce certifications, such as Administrator, Platform Developer, or Salesforce Life Sciences Cloud credentials. * Veeva Vault certifications or prior hands-on experience with Veeva CRM or Vault ...

TMF Lead

Malvern, PA · On-site

$32.75 - $45/hr

Configure and administer the Veeva Vault eTMF system for assigned studies, including user access/role management, metadata and document classification, workflow configuration, and support for system ...

TMF Lead

Malvern, PA · On-site

$32.75 - $45/hr

Configure and administer the Veeva Vault eTMF system for assigned studies, including user access/role management, metadata and document classification, workflow configuration, and support for system ...

TMF Lead

Malvern, AR · On-site

$29.25 - $40/hr

Configure and administer the Veeva Vault eTMF system for assigned studies, including user access/role management, metadata and document classification, workflow configuration, and support for system ...

Showing results 41-60

Veeva Vault Administrator information

What is a Veeva Vault Administrator?

A Veeva Vault Administrator is responsible for managing and configuring Veeva Vault, a cloud-based content and data management platform primarily used in the life sciences industry. They handle user access, security roles, system configurations, and workflow automation to ensure compliance with industry regulations. Additionally, they troubleshoot system issues, support end-users, and collaborate with business stakeholders to optimize Vault's functionality. Their role is crucial in maintaining data integrity and ensuring seamless document and quality management within the organization.

What are the typical daily responsibilities of a Veeva Vault Administrator?

As a Veeva Vault Administrator, your daily tasks include managing user access, configuring system workflows, troubleshooting technical issues, and maintaining data integrity and security within the platform. You will also routinely support end users, coordinate with IT and compliance teams to ensure system upgrades and validation, and help maintain alignment with industry regulations. This role often requires proactive monitoring and timely resolution of ticketed requests, as well as participation in periodic audits and training sessions. Your work ensures seamless document management and compliance for your organization’s regulated processes.

What are the key skills and qualifications needed to thrive as a Veeva Vault Administrator?

To thrive as a Veeva Vault Administrator, you need expertise in document management systems, compliance processes, and a strong understanding of life sciences regulations, typically supported by experience with Veeva Vault and related training or certifications. Familiarity with tools such as Veeva Vault QMS, Veeva Vault RIM, user management, and workflow configuration is often essential, with Veeva Administrator Certification being highly regarded. Excellent problem-solving, communication, and attention to detail are critical soft skills for efficiently supporting users and ensuring system integrity. These skills are crucial for maintaining regulatory compliance and optimizing business operations within life sciences organizations.

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What states have the most Veeva Vault Administrator jobs?

States with the most job openings for Veeva Vault Administrator jobs include:

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For Veeva Vault Administrator jobs, the most frequently searched job titles are:

Infographic showing various Veeva Vault Administrator job openings in the United States as of September 2026, with employment types broken down into 84% Full Time, 13% Contract, and 3% Nights. Highlights an 84% In-person, 3% Hybrid, and 13% Remote job distribution.

Sr. Manager, RIM Systems and Publishing

San Diego, CA • Remote

Bristol-Myers Squibb
Scientific Research and Development Services • 10K+ employees

$164K - $199K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz


Job description

Life at BMS At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer.

Here, you'll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact-on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/ Job Title: Sr

Manager, RIM Systems and Publishing Department: Regulatory Location: Remote FLSA Status: Exempt Job Responsibilities 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. Education and Experience 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. Skills and Qualifications 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. Excellent professional ethics and integrity. Physical Demands 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. #LI-REMOTE We hire for skills and capabilities, not just credentials - if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.

Compensation Overview: Remote - United States - US: $149,860 - $181,595 San Diego - CA - US: $164,846 - $199,754 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully - carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring.

Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance. Benefits: Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans - including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).

U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs

Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day. U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits RayzeBio and Bristol Myers Squibb 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. Supporting People with Disabilities 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. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement

Candidate Rights BMS and RayzeBio will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms.com with the Job Title and Requisition number. Do not send application-related inquiries to this email

To check your application status, please login to your Candidate Home Account. R1605077 : Sr. Manager, RIM Systems and Publishing.


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About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US