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Remote Pharmaceutical Editor Jobs (NOW HIRING)

Pacelabs

Proposal Writer - Life Sciences

$65K - $75K/yr

This is a full-time, remote, Monday through Friday, 8:30 a.m. - 5:00 p.m. Life Sciences Proposal ... Qualifications Education Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences ...

New

Inizio Evoke

Copy Supervisor

New York, NY · Remote

This is a fully remote role expected to support East Coast working hours. What You'll Do * Take ... A meticulous editor , ensuring clarity, accuracy, and consistency in all content. * A collaborative ...

Flywheel Partners

Medical Writer

Manhattan, NY · On-site +1

$65K - $85K/yr

We partner with pharmaceutical, medical device, and biotech companies to drive enhanced clinical ... Referencing, proofreading, and copy editing skills * High proficiency in Microsoft Word and ...

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How much do remote pharmaceutical editor jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for remote pharmaceutical editor in the United States is $41.22, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $50.24 per hour, depending on experience, location, and employer.

What is a remote pharmaceutical editor?

Remote Pharmaceutical Editors are professionals who review, revise, and ensure the accuracy of written materials related to pharmaceuticals, such as scientific manuscripts, regulatory documents, and marketing content, all while working from a remote location. They check for clarity, compliance with industry standards, and correct use of medical terminology. These editors often collaborate with scientists, researchers, and pharmaceutical companies to ensure that all documentation meets regulatory and publication requirements. Their expertise helps maintain high-quality communication within the pharmaceutical industry, even when working offsite.

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

To thrive as a Remote Pharmaceutical Editor, you need a robust background in life sciences or pharmacy, excellent written communication skills, and experience in scientific editing or medical writing. Familiarity with editing tools like Microsoft Word, reference management systems, and adherence to style guides such as AMA or ICMJE is typically required. Attention to detail, time management, and the ability to collaborate virtually with medical professionals and researchers are key soft skills for this role. These skills ensure the delivery of accurate, clear, and compliant pharmaceutical content that upholds scientific integrity in a remote work environment.

What are some common challenges faced by remote pharmaceutical editors when collaborating with cross-functional teams?

Remote pharmaceutical editors often collaborate with medical writers, regulatory professionals, and subject matter experts across different time zones and locations. A common challenge is ensuring clear and timely communication, especially when reviewing complex scientific documents under tight deadlines. Effective use of collaborative tools, regular virtual meetings, and proactive clarification of feedback can help mitigate misunderstandings and maintain project momentum. Building strong working relationships remotely is crucial for maintaining the accuracy and integrity of pharmaceutical content.
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Remote Pharmaceutical Editor jobs near you
Infographic showing various Remote Pharmaceutical Editor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $85,736 per year, or $41.2 per hour.

Associate Regulatory Affairs Labeling Associate

Civica Rx

Lehi, UT • On-site, Remote

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Job Description

Our Regulatory Affairs team brings essential generic quality medicines to U.S. patients by providing Regulatory leadership and establishing regulatory systems and processes that support Civica’s mission.

The Associate, Regulatory Affairs Labeling and Artwork (remote position):

·       Supports all aspects of product labeling and artwork development, review, approval, implementation and maintenance for Civica’s private label distribution (PLD) products.

·       Follow labeling and artwork procedures that comply with FDA, GMP, ISO and other applicable standards and regulations.

·       Coordinates and prepares Office of Prescription Drug Promotion (OPDP) submissions as needed.

·       Works within systems to maintain labeling and artwork.

·       Owns or impact assesses change controls for PLD labeling impact.

Responsibilities Include:
·       Coordinate labeling and artwork design by an external vendor

·       Collaborate with the supply chain, contract manufacturers, packagers, and external vendors to ensure timely implementation of approved labeling changes.

·       Maintain labeling and artwork records within applicable electronic systems and document repositories.

·       Support preparation and submission of Office of Prescription Drug Promotion (OPDP) materials, as needed.

·       Maintain FDA drug listings information and associated regulatory records.

·       Participate in change control activities as a change owner, contributor, or impact assessor, as appropriate, to evaluate and implement labeling-related changes.

·       Review labeling components and artwork for accuracy, consistency, completeness, and compliance with approved regulatory content.

·       Ensure labeling information included in regulatory submissions is complete, accurate, and consistent.

·       Support continuous improvement initiatives related to labeling processes, systems, and workflows.

·       Perform any other tasks/duties as assigned by management.

What we look for:

We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue doing what is in the best interest for our patients.

Technical Skills;

Proven experience in critically reviewing documents for consistency and accuracy. Excellent proofreading/editing skills are required.

Strong organizational skills.

Demonstrated superior oral and written communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner. Strives to continuously improve and build knowledge and skills.

Teamwork:

Balances team and individual responsibilities; Exhibits objectivity and openness to others' views; Gives and welcomes feedback; Contributes to building a positive team spirit; Inspires respect and trust.

Quality Management:

Looks for ways to improve and promote quality; Demonstrates accuracy and thoroughness.

Education Minimum Requirement :

Bachelor’s degree required, focus in Life Sciences preferred.

Required Experience and Skills :

At least one to two 2+ years of relevant experience within the pharmaceutical regulatory environment, with a concentration in pharmaceutical labeling and/or artwork development or promotional review.

Physical demands of the position include only those required for work in a typical office environment. Minimal travel (0-5%) may be necessary in the execution of the listed duties

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About Civica Rx

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

51 - 200 Employees

Headquarters location

Lehi, UT, US

Year founded

2018

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