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Pharmaceutical Proofreading Jobs (NOW HIRING)

The ideal candidate has experience in either pharmaceutical manufacturing/process support or ... Perform data entry, data checks, proofreading, and document review activities to support accurate ...

New

... outlining and proofreading. Skills: * Strong background in technical writing of Quality controlled documents in the pharmaceutical/biotechnological industry. * Strong communication skills.

... Chemical, Biotech, & Pharmaceutical practice team. The right candidate will provide legal ... Provide document production services, including styling and formatting of documents; proofreading ...

... device, and pharmaceutical organizations of all sizes to confidently advance scientific ... Pharmacy degree Excellent verbal and written communication skills, including proofreading ...

... pharmaceutical industry. * The ability to understand clinical trial data, methodologies, and complex research. * Exceptional writing, editing, and proofreading skills. * The ability to work ...

Marketing Internship

Exton, PA · On-site

$14.50 - $19.25/hr

Contribute to copywriting, proofreading, and editing of marketing materials including press releases, blog posts, and social media content * Research pharmaceutical market trends, competitor activity ...

Showing results 41-60

Pharmaceutical Proofreading information

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$13

$27

$43

How much do pharmaceutical proofreading jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for pharmaceutical proofreading in the United States is $27.65, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $33.65 per hour, depending on experience, location, and employer.

What is pharmaceutical proofreading?

Pharmaceutical proofreading is the process of carefully reviewing pharmaceutical documents, such as drug labels, research papers, clinical trial reports, and marketing materials, to ensure accuracy, clarity, and compliance with regulatory standards. Proofreaders check for errors in spelling, grammar, and formatting, as well as verifying scientific terminology and data consistency. This role is critical in the pharmaceutical industry because mistakes in documentation can lead to regulatory issues, miscommunication, or even patient safety risks. Pharmaceutical proofreaders often work closely with medical writers, regulatory teams, and subject matter experts. Their work helps maintain the credibility and reliability of pharmaceutical communications.

What are the key skills and qualifications needed to thrive as a pharmaceutical proofreader?

To thrive as a Pharmaceutical Proofreader, you need a keen eye for detail, strong knowledge of medical terminology, and a background in life sciences or pharmaceutical studies. Familiarity with regulatory documentation systems, style guides, and proofreading tools such as Adobe Acrobat or Microsoft Word's track changes is essential. Excellent organizational skills, time management, and the ability to communicate clearly with cross-functional teams are standout soft skills. These competencies ensure accuracy, regulatory compliance, and clear communication in pharmaceutical documentation, which are critical for patient safety and product approval.

What are some common challenges pharmaceutical proofreaders face when reviewing scientific documents?

Pharmaceutical proofreaders often encounter challenges such as deciphering complex scientific terminology, ensuring regulatory compliance, and maintaining consistency across multiple document versions. They must pay close attention to detail to catch subtle errors in drug names, dosages, and data presentations, as even minor mistakes can have significant consequences. Effective communication and collaboration with medical writers, regulatory teams, and subject matter experts are also crucial, as proofreaders frequently clarify ambiguities or resolve discrepancies within tight deadlines.

What is the difference between Pharmaceutical Proofreading vs Medical Writer?

AspectPharmaceutical ProofreadingMedical Writer
Required CredentialsTypically a degree in life sciences, pharmacy, or related field; strong language skillsOften a degree in life sciences, journalism, or communications; writing expertise
Work EnvironmentPharmaceutical companies, CROs, or freelance; focus on document reviewPharmaceutical, biotech, or healthcare companies; focus on creating and editing content
Employer & Industry UsageUsed for ensuring accuracy in regulatory documentsUsed for developing scientific content, regulatory submissions, and publications

Pharmaceutical Proofreading primarily involves reviewing and correcting regulatory documents for accuracy and compliance, while Medical Writers create and develop scientific content. Both roles require strong scientific knowledge and attention to detail, but differ in their core responsibilities and output.

How to become a pharmaceutical proofreader?

To become a pharmaceutical proofreader, candidates typically need a strong background in life sciences or pharmacy, along with excellent attention to detail and knowledge of medical terminology. A bachelor's degree in a related field is often required, and proficiency with editing tools and understanding of regulatory guidelines are beneficial. Gaining experience through internships or entry-level editing roles can also improve job prospects.
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What cities are hiring for Pharmaceutical Proofreading jobs?

Cities with the most Pharmaceutical Proofreading job openings:

What states have the most Pharmaceutical Proofreading jobs?

States with the most job openings for Pharmaceutical Proofreading jobs include:

What job categories do people searching Pharmaceutical Proofreading jobs look for?

The top searched job categories for Pharmaceutical Proofreading jobs are:

Infographic showing various Pharmaceutical Proofreading job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $57,520 per year, or $27.7 per hour.

Medical Writer

Chesterfield, MO

Contractor

Re-posted 21 days ago


Job description

Company Description

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.

As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.

Job Description

The BRD organization within the Pharm Sci BTx organization needs to hire a technical writer. This colleague will perform the following activities:

  • Assist with verification of data within regulatory documents or reports.
  • Support the bioprocess R&D (BRD) teams in tracking document completion, data verification strategies and completion of edits.
  • Create drafts of new technical or regulatory documents using existing examples, templates or reports
  • Assist Bioprocess team authors in assembling, formatting, and proofreading figures, tables and content.
Qualifications

SKILLS:

  • Excellent oral and written communications with experience in technical writing of reports and/or regulatory documents
  • Regulatory, GMP or Pharmaceutical experience, preferrably in bioprocess or cell line development areas is desirable
  • Detail oriented

EXPERIENCE:

  • 3-5 years

EDUCATION:

  • Scientific Background; BS or higher Biology, Chemistry, Biochemistry, Molecular Biology, Engineering, or similar
Additional Information

All your information will be kept confidential according to EEO guidelines.


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