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Remote Pharmaceutical Editor Jobs (NOW HIRING)

... Pharmaceuticals ) team within our Philadelphia office to develop life-changing and in many cases ... While this position will report into our Philadelphia location, due to our current remote capacity ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Assure quality in the supply chains of various clients within the animal health, pharmaceutical ...

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Remote Pharmaceutical Editor information

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How much do remote pharmaceutical editor jobs pay per hour?

As of Jun 9, 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 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.

What are Remote Pharmaceutical Editors?

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, and why are they important?

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.
More about Remote Pharmaceutical Editor jobs
What cities are hiring for Remote Pharmaceutical Editor jobs? Cities with the most Remote Pharmaceutical Editor job openings:
What are the most commonly searched types of Pharmaceutical Editor jobs? The most popular types of Pharmaceutical Editor jobs are:
What states have the most Remote Pharmaceutical Editor jobs? States with the most job openings for Remote Pharmaceutical Editor jobs include:
What job categories do people searching Remote Pharmaceutical Editor jobs look for? The top searched job categories for Remote Pharmaceutical Editor jobs are:
Infographic showing various Remote Pharmaceutical Editor job openings in the United States as of June 2026, with employment types broken down into 82% Full Time, and 18% Contract. Highlights an 100% Remote job distribution, with an average salary of $85,736 per year, or $41.2 per hour.
Remote Analytical SME & CMC Technical Writer

Remote Analytical SME & CMC Technical Writer

Sigma Systems, Inc.

Ridgefield, CT โ€ข On-site, Remote

Full-time

Posted 6 days ago


Job description

37278373 Remote Analytical SME & CMC Technical Writer,ย 12 Months
Sigma Systems is seeking an Analytical SME & CMC Technical Writer to work remote

We are seeking an experienced Analytical Subject Matter Expert (SME) and CMC Technical Writer to support external drug substance (DS) and drug product (DP) development programs within External Alternative CMC development (EACD) at Boehringer Ingelheim.
This contract role combines deep expertise in DS/DP analytical development and quality control to support ongoing DS/DP external CMC development and demonstrated familiarity of Veera RIM system and technical writing capabilities to support documentation and global regulatory submissions (e.g., IND, CTA, NDA/MAA).
The successful candidate will collaborate with internal cross-functional teams and external partners (CDMOs/CROs) to ensure scientifically robust analytical strategies and clear, compliant CMC documentation aligned with global regulatory expectations.

Responsibilities:
Analytical Expertise

  • Provide scientific leadership in phase appropriate external DS/DP analytical development/QC for NCE and NCE-like (e.g., Oligonucleotide) entities, including method development, validation, transfer and lifecycle management
  • Contribute to development of DS/DP phase appropriate specifications and analytical control strategies in collaboration with internal and external teams
  • Contribute to development of DS/DP stability programs and assignment of DS retest period, DP shelf life and material holding times as needed, with internal and external teams to support FIH and following clinical trials
  • Independently propose or review quality agreement, SOW, study protocols/reports, batch/stability data, to support CMC deliverables in a timeline fashion.
  • Prepare and communicate clearly and independently technical plans, updates and deliverables as needed in the form of reports and/or presentations within the internal teams
  • Partner with internal teams and external vendors (CDMOs/CROs) to resolve technical challenges and quality events and ensure timely, compliant deliverables

CMC Technical Writing

  • Support departmental submission activities by managing documentation workflow workflow in Veeva RIM system
  • Demonstrated working experience in authoring, reviewing and editing (content and format) CTD Module 3 (Drug Substance and Drug Product) documents, in particular analytical related documents.
  • Contribute to preparation of regulatory submissions/briefings and responses to health authority inquirie

Requirements:

  • Advanced degree (e.g., PhD) is preferred, or Master's and Bachelor's degree in Analytical Chemistry, Pharmaceutical Sciences, or related discipline
  • Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical development of NCE and NCE-like drug substance and solid and liquid formulations.
  • Demonstrated working experience in regulatory submissions
  • Familiarity with GMP and regulatory guidelines (e.g., ICH, FDA, EMA, USP, EP, etc.)

Preferred

  • Experience in global regulatory submissions (IND, CTA, NDA, MAA)
  • Experience working with external manufacturing or testing partners

Key Skills

  • Strong organization and technical writing skills
  • High attention to detail and scientific rigor
  • Effective communication and stakeholder collaboration
  • Ability to manage multiple priorities in a fast-paced environment