Full-Time

Veeva Quality Vault Business Administrator

Quality Assurance

Posted on 9/10/2025

Celerion

Celerion

1,001-5,000 employees

Global CRO for early-phase development

No salary listed

Remote in USA

Remote

Category
Medical, Clinical & Veterinary (1)
Requirements
  • Associate’s degree in a related field; Bachelor’s degree preferred; or a combination of education and experience.
  • At least 1 year of experience configuring a product built off the Veeva Vault platform.
  • At least 3 years of experience with process and/or training development.
  • Ability to document processes, multitask and manage multiple ongoing projects.
  • Highly organized, motivated, able to problem-solve, and learn quickly.
  • Ability to work effectively across all levels of the organization.
Responsibilities
  • Monitor system performance and usage, ensuring the platform is running efficiently and addressing any issues promptly.
  • Oversee and manage Training Matrix. Coordinate periodic reviews of curricula and learner roles.
  • Develop, set up, and revise data access controls and permission levels to ensure data security and integrity. Build and manage user accounts for those without login accounts.
  • Create reports and dashboards for management to assist in monitoring access, use, and to support audits/inspections.
  • Ensure compliance with organizational policies and best practices for training and document control records management.
  • Act as a point of contact for Veeva Quality Suite related queries and issues within the organization.
  • Provide technical support to end-users, triaging and troubleshooting issues with timely resolution.
  • Collaborate with Veeva support and technical teams as needed for complex issues.
  • Develop and facilitate continuing education for Training Administrators.
  • Develop and deliver training materials to support the adoption of Veeva Quality Suite within the organization, and maintain up-to-date documentation as the system evolves.
  • Identify opportunities to optimize system usage and performance.
  • Work closely with stakeholders and internal teams to understand their needs, goals, and system requirements.
  • Support the development of implementation plans outlining the steps, timelines, and resources required to deploy training solutions successfully.
  • Assist with migrating data and/or processes from legacy systems or into Veeva Quality Suite.
  • Perform thorough testing of Veeva Quality to ensure they meet quality standards and fulfill the organization's requirements. Identify and resolve any issues or bugs and iterate on the solution as needed to improve performance and usability.
Desired Qualifications
  • Life sciences experience preferred.
  • Vault Training Administrator and Veeva Associate/Certified Administrator credentials are a plus.

Celerion is a global contract research organization focused on early-phase drug development. It supports pharmaceutical and biotech clients with trial design, feasibility, project management, clinical and medical monitoring, bioanalytical sciences, and regulatory affairs, all conducted under contract. Its work hinges on metabolite profiling using high-resolution mass spectrometry to inform development decisions. With 40+ years of experience and a global, integrated service network, Celerion aims to help clients bring safe, effective treatments to patients faster by delivering rigorous, timely research.

Company Size

1,001-5,000

Company Stage

Acquired

Total Funding

N/A

Headquarters

Lincoln, Nebraska

Founded

2010

Simplify Jobs

Simplify's Take

What believers are saying

  • THL Partners acquisition in 2026 funds geographic expansion and technology upgrades.
  • Jo Goodman’s 29-year expertise from AstraZeneca drives bioanalytical innovation.
  • CLIA certification enables high-complexity diagnostic testing on human specimens.

What critics are saying

  • Labnotes fails against Veeva, causing client exodus in 12-18 months.
  • THL debt strains cash flow, forcing service cuts in 6-12 months.
  • CMS revokes CLIA due to Lincoln lab overload in 18-24 months.

What makes Celerion unique

  • Celerion excels in HRMS metabolite profiling for early-phase drug development.
  • Labnotes software streamlines bioanalytical data management with advanced dataset tools.
  • GLP/GCP molecular testing including ELISpot and qPCR accelerates cell/gene therapies.

Help us improve and share your feedback! Did you find this helpful?

Benefits

Flexible Work Hours

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

1%

2 year growth

4%
PharmiWeb.com
May 7th, 2025
Celerion Launches Enhanced Version Of Labnotes Bioanalytical Data Management Software

LINCOLN, Neb.; May 6, 2025 (Business Wire) – Celerion, a global leader in early clinical research and bioanalytical services, announced the launch of the latest version of Labnotes, its cutting-edge bioanalytical electronic laboratory notebook software elevating data handling and analysis capabilities for sponsors. The latest system enhancements streamline laboratory documentation and improve operational efficiency for users. The updated platform also offers advanced tools for handling and organizing large datasets, ensuring faster processing of reports and optimized database queries

Instrument Business Outlook
May 6th, 2025
Celerion Launches Enhanced Version of Labnotes Bioanalytical Data Management Software

Celerion launches enhanced version of labnotes bioanalytical data Management software.

Business Wire
Jun 5th, 2024
Celerion Honored With Prestigious CRO Leadership Award for Ninth Consecutive Year

Celerion was recognized as a CRO Leader in the quality, capabilities and reliability categories across two groups of respondents (small pharma and combined big and small pharma).

Business Wire
May 7th, 2024
Jo Goodman Joins Celerion as Vice President of Bioanalytical Services

Celerion announced the appointment of Jo Goodman as vice president of bioanalytical services in its Lincoln, Nebraska, laboratory.Post this

Business Wire
May 7th, 2024
Jo Goodman Joins Celerion As Vice President Of Bioanalytical Services

LINCOLN, Neb.--(BUSINESS WIRE)--Celerion, a leading clinical research organization, specializing in early clinical research and bioanalytical services, today announced the appointment of Jo Goodman as vice president of bioanalytical services in its Lincoln, Nebraska, laboratory. In her new role, Goodman will oversee the strategic direction and operational performance of the Lincoln bioanalytical laboratory, leveraging her extensive experience in pharmaceutical research and development to drive innovation and design and execute customized bioanalysis for clients’ needs. She will be responsible for delivering on Celerion’s bioanalytical promise of industry-leading science, stringent compliance, and speed of delivery. With over 29 years of experience in the pharmaceutical industry, Goodman brings a wealth of knowledge in regulated GxP and discovery bioanalysis for both in-house and outsourced activities. Prior to joining Celerion, she held positions of increasing responsibility at AstraZeneca, MedImmune, and GlaxoSmithKline. Additionally, Goodman is a recognized thought leader, having recently served as a member of the Expert Working Group (EWG) for ICH M10 Bioanalytical Guidance Development and is active in numerous non-profit industry consortia such as EBF, AAPS, and DMDG

INACTIVE