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Temp Veeva Jobs (NOW HIRING)

Randstad

Validation Engineer

Thousand Oaks, CA · On-site

$60 - $74/hr

GMP * Engineering * technical writing * validations * veeva * Computer System Validation ... Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one ...

AllSTEM Connections

Document Controller

Indianapolis, IN · On-site

$72K - $85K/yr

Required hands-on experience with Veeva QualityDocs. * Domain Knowledge: Detailed understanding of ... For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major ...

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Temp Veeva information

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How much do temp veeva jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for temp veeva in the United States is $25.72, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $34.13 per hour, depending on experience, location, and employer.

What is a Temp Veeva?

A Temp Veeva is a temporary employee or contractor who works with Veeva Systems software, which is widely used for cloud-based solutions in the life sciences industry. These professionals typically assist with implementing, managing, or supporting Veeva applications such as Veeva Vault, CRM, or QualityDocs. Temp Veeva workers may be hired for short-term projects, system migrations, or to cover workforce gaps. Their responsibilities can include data entry, system configuration, user support, or training. This role is ideal for individuals with experience in pharmaceutical regulations, software administration, and project management.

What are the key skills and qualifications needed to thrive as a Temp Veeva specialist, and why are they important?

To thrive as a Temp Veeva Specialist, you need a strong understanding of Veeva Vault applications, data management, and relevant industry regulations, typically paired with experience in life sciences or pharmaceuticals. Familiarity with Veeva Vault platforms, document management systems, and possibly certifications such as Veeva Administrator or related credentials is highly valuable. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for ensuring data quality and collaborating with cross-functional teams. These skills and qualifications are vital to maintain compliance, streamline processes, and support efficient document and data management in regulated environments.

What are some common challenges Temp Veeva professionals face when working with new teams or clients?

Temp Veeva professionals often face the challenge of quickly adapting to different organizational processes and compliance standards, as each client may have unique configurations of the Veeva platform. Additionally, they must rapidly build rapport with new teams and stakeholders to facilitate smooth onboarding and project execution. Effective communication and a proactive approach to learning the nuances of each environment are essential for overcoming these challenges and delivering value efficiently.

What is the difference between Temp Veeva vs Veeva Administrator?

AspectTemp VeevaVeeva Administrator
CertificationsVeeva certifications often preferredVeeva certifications required
Work EnvironmentTemporary, project-based rolesFull-time, ongoing support roles
Industry UsageUsed in clinical, regulatory, commercial projectsPrimarily in life sciences companies managing Veeva systems

Temp Veeva roles are typically short-term, project-focused positions requiring familiarity with Veeva systems, while Veeva Administrator roles are permanent positions involving ongoing system management and support. Both roles demand Veeva certifications and industry experience, but differ mainly in duration and scope of responsibilities.

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Temp Veeva jobs near you
Infographic showing various Temp Veeva job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 1% Part Time, 1% Temporary, and 10% Contract. Highlights an 70% Physical, 7% Hybrid, and 23% Remote job distribution, with an average salary of $53,499 per year, or $25.7 per hour.

Regulatory Writer and/or Regulatory QC/ Editor (Temporary)

Vir Biotechnology

Remote

$90 - $120/hr

Temporary

Re-posted 11 days ago

Job description

THE OPPORTUNITY

Vir Biotechnology is looking for a Regulatory Writer (Temporary) who will support the quality, consistency, and accuracy of regulatory documents produced by the Regulatory Writing team by either functioning as a support author and/or by focusing on editorial and QC review of documents written by other team members. Reporting to the Senior Director, Regulatory Writing, you will help ensure accuracy, compliance, and consistency of regulatory submission materials by partnering closely with medical writers, regulatory affairs, clinical, biostatistics, and other crossfunctional stakeholders.

WHAT YOU'LL DO
  • In partnership with an experienced lead author, write and edit a wide range of regulatory documents, including but not limited to: Clinical trial protocols and amendments, Investigator Brochures (IBs), Clinical Study Reports (CSRs), briefing packages, and components of regulatory submission dossiers (eg, NDA, IND, MAA)
  • Perform independent QC reviews of documents produced by the regulatory writing function
  • Verify the accuracy and internal/external consistency of documents versus their source materials
  • Define and confirm the scope of QC activities with document authors; identify required source documents/data and ensure availability prior to QC start
  • Review documents for adherence to applicable style guides (eg, AMA Manual of Style and internal style/formatting standards), templates, and regulatory guidance, identify and document discrepancies and recommended corrections
  • Proofread and copyedit text to ensure clarity, grammar, spelling, punctuation, and consistency of messaging/presentation, while preserving scientific and regulatory accuracy
  • Support preparation and inspectionreadiness of technical documents for global regulatory submissions (eg, eCTD/CTD), including integration of narrative text, tables, graphs, charts, and statistical output
  • Communicate QC findings clearly and constructively to medical writers and other stakeholders; collaborate to resolve issues and support timely completion of deliverables
  • Facilitate the efficient project management of individual document workflows (from KOM through handoff to publishing) and contribute to departmental trackers and integrated timelines. Communicate status and progress to stakeholders, participating in cross-functional meetings when needed
  • Contribute to the continuous improvement of QC tools, checklists, and processes; provide feedback on SOPs, work instructions, and best practices for regulatory document quality
WHO YOU ARE AND WHAT YOU BRING
  • Bachelor's degree and 5 plus years of relevant experience. Advanced degree in science or medical field is a plus
  • Working knowledge of the industry and content of key eCTD documents, familiarity with CTD/eCTD structure and common templates
  • Understanding of drug development and regulatory submission processes, including familiarity with ICH guidelines and major health authority expectations (eg, FDA, EMA)
  • Exceptional attention to detail with strong analytical and criticalthinking skills, including the ability to identify inconsistencies, data issues, and deviations from standards
  • Proven ability to manage multiple tasks and priorities in a deadlinedriven environment, operating with a high degree of independence and accountability
  • Experience working crossfunctionally in collaborative team environments and building effective working relationships with authors, reviewers, and project teams
  • Experience with electronic document management and publishing systems (eg, Veeva Vault)
  • Experience with project and timeline management systems (eg, SmartSheet)
#LI-AS1
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WHO WE ARE AND WHAT WE OFFER

The expected hourly range for this position is $90.00 to $120.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.

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