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Pharmaceutical Document Review information

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$13

$23

$33

How much do pharmaceutical document review jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for pharmaceutical document review in the United States is $23.33, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $26.92 per hour, depending on experience, location, and employer.

What is the difference between Pharmaceutical Document Review vs Clinical Document Reviewer?

AspectPharmaceutical Document ReviewClinical Document Reviewer
Required CredentialsTypically requires life sciences degree, regulatory knowledge, and attention to detailRequires clinical research background, regulatory familiarity, and detail orientation
Work EnvironmentPharmaceutical companies, CROs, regulatory agenciesClinical trial sites, CROs, pharmaceutical firms
Industry UsageUsed for reviewing regulatory submissions, SOPs, and manufacturing documentsFocuses on reviewing clinical trial documents, case report forms, and patient data

Both roles involve detailed document review within the pharmaceutical industry, but Pharmaceutical Document Review primarily focuses on regulatory and manufacturing documents, while Clinical Document Review centers on clinical trial data and patient records. They share similar skills and work environments but serve different stages of drug development and regulatory processes.

What cities are hiring for Pharmaceutical Document Review jobs?

Cities with the most Pharmaceutical Document Review job openings:

What are popular job titles related to Pharmaceutical Document Review jobs?

For Pharmaceutical Document Review jobs, the most frequently searched job titles are:

6507 - Document Controller / Associate CQV Engineer

West Chester, OH • On-site

Verista, Inc.
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Verista, Inc.external

Full-time

Posted 11 days ago

Job description

We are seeking an experienced Document Controller to support document management and control activities within a regulated pharmaceutical manufacturing environment. This individual will be responsible for maintaining accurate, compliant, and controlled documentation while supporting Quality, Engineering, Validation, Manufacturing, and other cross-functional teams.

Document Controller Responsibilities
  • Manage the creation, routing, review, approval, issuance, revision, and archival of controlled documents within the electronic document management system (EDMS).
  • Utilize Veeva to manage document workflows, approvals, revisions, and document lifecycle activities.
  • Ensure controlled documents are accurate, current, properly formatted, and maintained in accordance with established procedures and cGMP requirements.
  • Support document control activities for SOPs, work instructions, specifications, protocols, reports, forms, and other GxP documentation.
  • Coordinate document reviews and approvals with Quality, Engineering, Validation, Manufacturing, and other stakeholders.
  • Track documents through the approval process and follow up with document owners and reviewers to ensure timely completion.
  • Maintain document histories, revision records, effective dates, and appropriate archival of superseded documentation.
  • Perform quality checks of documentation for completeness, accuracy, formatting, and compliance with Good Documentation Practices (GDP).
  • Assist with document retrieval and preparation for internal audits, regulatory inspections, and project activities.
  • Support continuous improvement of document control processes and procedures.
Requirements
  • Previous Document Control experience within the pharmaceutical, biotechnology, or other highly regulated life sciences industry required.
  • Hands-on experience with Veeva, preferably Veeva Vault QualityDocs or a similar Veeva document management application, required.
  • Knowledge of cGMP and Good Documentation Practices (GDP).
  • Experience managing controlled documents and electronic document workflows.
  • Strong attention to detail with excellent organizational and time-management skills.
  • Ability to manage multiple documents, priorities, and deadlines simultaneously.
  • Strong written and verbal communication skills with the ability to work effectively across multiple functional groups.
  • Proficiency with Microsoft Office applications.
  • Ability to work onsite in West Chester, Ohio.

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