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Sarah Jenkins
Remote Medical Editor jobs in the United States
Job type
Min. salary, $/year
Level
The demand for skilled medical editor remote jobs continues to grow across the USA as healthcare organizations, publishers, and research institutions seek accurate, polished content. Currently, 500+ positions are open, reflecting the increasing need for professionals who can refine complex clinical material. This role offers a flexible work setup for candidates ready to make a nationwide impact on healthcare communication.
Successful candidates bring strong command of clinical terminology, exceptional attention to detail, and the ability to interpret complex data within manuscripts, journals, and regulatory documents. Familiarity with AMA style guidelines, proofreading software, and evidence-based writing practices is highly valued. Employers seeking to hire a medical editor often prioritize candidates with a background in life sciences, pharmacology, or healthcare communications, paired with excellent collaboration and time-management skills suited for independent work.
Medical editor positions in the USA typically involve collaborating with writers, researchers, and subject matter experts through digital platforms, ensuring consistency and compliance with industry standards. As telehealth and digital publishing expand, companies increasingly embrace remote arrangements, broadening access to talent beyond traditional office hubs. This shift fuels steady demand for experienced professionals who can adapt to evolving healthcare communication needs nationwide.
If you're ready to advance your career and contribute to high-quality healthcare content, explore the latest medical editor vacancies available through Global Work AI. Take the next step toward a flexible, rewarding career by connecting with employers eager to hire dedicated editing professionals today.
IQVIA Language Solutions
Translate, post-edit, and review clinical trial documentation to ensure compliance with medical and ethical standards. Enhance readability and accuracy of scientific materials while maintaining original meaning.
remote (anywhere)Full TimeJunior (<2 years)
McGraw Hill LLC.
Deliver high-quality developmental and substantive editing of medical content, ensuring clarity, structure, and pedagogical effectiveness. Manage multiple content projects, maintaining timelines and quality standards.
remote, United States$62k – $117k/yrFull TimeSenior (5+ years)
HJ Staffing
Conduct Peer-to-Peer (P2P) reviews with treating physicians regarding authorization requests. Analyze clinical documentation and evaluate medical necessity and level of care. Apply CMS Medicare Advantage requirements and clinical criteria. Document P2P discussions and maintain HIPAA compliance.
remote, United StatesFull TimeLead / Manager
Mindrift
Evaluate clinical EHR vignettes for accuracy and completeness, assess clinical reasoning quality, and score benchmark items based on established criteria. Conduct independent blind reads and participate in physician adjudication to ensure quality and correctness of clinical cases.
remote, United States$101k/yrPart TimeJunior (<2 years)
Inspira Education
Guide medical school candidates in building their profiles and drafting application materials. Manage relationships with applicants and families, providing strategic guidance on school selection, essays, resumes, and interviews.
remote, United StatesPart TimeJunior (<2 years)
Oscar Health
Provide strategic leadership to the Clinical Policy team, ensuring evidence-based medical and pharmacy policies. Manage the full policy lifecycle, lead clinical research, and advise on emerging medical therapies.
remote, United States$238k – $312k/yrFull TimeDirector
Praxis Precision Medicines, Inc.
Prepare and submit accurate MLR submission packages in Veeva RAPID, ensuring all supporting documentation is organized and linked correctly. Perform quality assurance checks in Veeva PromoMats, verifying that final materials match approved content.
remote, United States$95k/yrFull TimeJunior (<2 years)
Ripple Effect
Oversee production of technical reports and documents, ensuring quality and compliance. Manage timelines and budgets, assign writing tasks, and guide team output. Enforce editorial standards, conduct final reviews, and implement corrective actions.
remote, United States$89k – $102k/yrFull TimeSenior (5+ years)
Precision AQ
Lead content development for multiple medical communication projects, ensuring high quality and adherence to guidelines. Collaborate with internal teams and clients, review project briefs, and supervise medical writers.
remote, United States$120k – $160k/yrFull TimeDirectorAACN (American Association of Critical-Care Nurses)
Lead the editorial management of AACN-owned and contracted print and digital journals, overseeing preproduction, production, and postproduction phases. Collaborate with stakeholders to ensure content quality and compliance with publishing standards.
remote, United States$104k – $131k/yrFull TimeDirector
RTI International
Lead publication planning and development, collaborating with internal teams and external authors to produce high-quality medical communications. Manage publication workflows from concept to submission, ensuring compliance and quality control.
remote, CA, United States$95k – $105k/yrFull TimeSenior (5+ years)
Pillar4 Media
Edit product reviews, roundups, and informational stories to ensure content is engaging, accurate, and optimized for SEO. Collaborate with editorial and SEO teams to enhance content quality and performance. Manage freelance writers and medical reviewers, providing direction and feedback.
remote, CO, United StatesFull TimeLead / Manager
Princeton10
Edit and ensure regulatory compliance for pharmaceutical marketing materials. Fact-check and proof existing copy for various channels. Provide medical, regulatory, and legal expertise to maintain accuracy within FDA guidelines.
remote, AZ, United States$121k – $141k/yrFull TimeMiddle (2-4 years)IQVIA Language Solutions
Translate, post-edit, and review clinical trial documentation to ensure adherence to medical and ethical standards. Enhance readability and accuracy of scientific materials while maintaining original meaning.
remote, Colchester, CT, United StatesFull TimeJunior (<2 years)
Precision Medicine Group
Lead content development for medical communications across multiple therapeutic areas, ensuring high quality and adherence to guidelines. Collaborate with internal teams, review project briefs, and supervise medical writers.
remote, United States$110k – $145k/yrFull TimeDirectorThe Lockwood Group, LLC
Lead assigned accounts and client interactions, oversee scientific content development across therapeutic areas, manage resource allocation, and partner with client services to create statements of work and timelines.
remote, United StatesFull TimeDirectorPrecision AQ
Lead content development for medical communications across multiple therapeutic areas, ensuring high quality and adherence to guidelines. Collaborate with internal teams and clients, review project briefs, and supervise medical writers.
remote, United States$110k – $145k/yrFull TimeDirectorSaratoga Ascend
Conduct medical assessments of adverse events, ensuring compliance with FDA regulations. Review safety data trends and consult on safety reporting to regulatory bodies. Collaborate with study teams to address eligibility questions and protocol deviations.
remote, United StatesFull TimeSenior (5+ years)The Lockwood Group, LLC
Perform substantive editing, copyediting, and quality review of oncology and hematology educational materials. Manage timelines, deliverables, and editorial workflows while monitoring project status. Facilitate communication among stakeholders and maintain project trackers.
remote (anywhere)Full TimeSenior (5+ years)McGraw Hill LLC.
Lead the Physical Therapy and Allied Health portfolio, overseeing print and digital products. Establish relationships with educators and clinicians to identify market trends. Acquire new content and partnerships to support portfolio growth.
remote, United States$55k – $129k/yrFull TimeSenior (5+ years)
Public Library of Science
Oversee the editorial process for manuscripts submitted to PLOS journals, making complex editorial decisions based on evaluations and reviewer comments. Serve as a point of escalation for editorial queries and support teams to uphold scientific rigor.
remote, FL, United States$67k – $73k/yrFull TimeJunior (<2 years)
AdvanzPharma
Serve as the medical expert for Photofrin and Photodynamic Therapy (PDT). Develop relationships with healthcare professionals and key opinion leaders. Execute local Medical Affairs plans, lead medical education initiatives, and support clinical research activities.
remote, United States$128k – $158k/yrFull TimeMiddle (2-4 years)
Lumanity
Develop high-quality, scientifically accurate content for medical affairs and promotional medical education deliverables, including slide decks and presentations. Conduct literature searches and background research to ensure content accuracy.
remote, United StatesFull TimeJunior (<2 years)
Med-IQ
Develop clinical education content related to risk management, patient safety, and grants. Conduct literature searches, create educational materials, and collaborate with content writers and faculty experts. Manage freelance writers and ensure compliance with accreditation standards.
remote, United States$85k – $115k/yrFull TimeMiddle (2-4 years)McGraw Hill LLC.
Oversee day-to-day execution of author management, permissions tracking, and project coordination. Maintain project schedules, monitor risks, and ensure compliance with quality standards.
remote, United States$40k – $77k/yrFull TimeMiddle (2-4 years)
Avalere Health
Edit and proofread scientific and medical communications for accuracy and compliance with style requirements. Perform data checking to verify scientific claims and assess copyright permissions.
remote, Philadelphia, PA, United States$55k – $65k/yrFull TimeJunior (<2 years)
MJH Life Sciences®
Develop and maintain expertise in oncology and related therapeutic areas. Plan, write, edit, and review CME/CE-certified educational content for healthcare professionals. Lead core conferences and collaborate with teams to ensure compliance with ACCME standards.
remote, United States$120k – $130k/yrFull TimeDirectorThe Lockwood Group, LLC
Support Managing Editors by editing, proofreading, and checking data for various accounts. Maintain knowledge of style guidelines and contribute to updates of Editorial SOPs. Address editorial questions from team members and review content for grammatical standards and narrative coherence.
remote, CT, United StatesFull TimeSenior (5+ years)IQVIA Language Solutions
Translate, post-edit, and review clinical trial documentation to ensure compliance with medical and ethical standards. Enhance readability and accuracy of scientific materials while maintaining original meaning.
remote (anywhere)Full TimeJunior (<2 years)
Edera
Edit and proofread technical documents including manuals, product guides, and whitepapers. Collaborate with subject matter experts and product teams to ensure accuracy and clarity. Maintain documentation standards and manage version control.
remote, United StatesFull TimeMiddle (2-4 years)
Compass Pathways
Serve as a medical subject matter expert in treatment-resistant depression (TRD) and emerging psychiatric treatments. Evaluate clinical trial results and scientific literature to inform medical strategy.
remote, United States$270k – $320k/yrFull TimeDirector
Clinical Care Options LLC
Develop and manage content for CME and IME programs across various formats. Collaborate with expert faculty and freelancers, assign projects, and ensure quality and timely completion of deliverables. Participate in medical conferences and contribute to conference coverage programs.
remote, United StatesFull TimeDirector
Kaiva Corp
Format and proofread documents written by FDA scientists, ensuring consistency and adherence to style guides. Create and manage data tables using regulatory submission data, and maintain document templates.
remote, DC, United StatesFull TimeJunior (<2 years)Vaniam Group LLC
Ensure editorial accuracy and consistency across various materials including abstracts and manuscripts. Act as editorial lead on multiple projects, managing deadlines and deliverables. Leverage AI tools to enhance productivity and streamline workflows.
remote, United StatesFull TimeSenior (5+ years)
ECU Health Medical Center
Lead the Code Edit Analyst team, ensuring productivity and quality in claims processing. Conduct coding audits, monitor performance metrics, and provide training on coding updates and compliance.
remote, NC, United States$60k – $88k/yrFull TimeLead / Manager
Machinify
Source, design, validate, and maintain clinical and coding content for claims editing products. Monitor authoritative sources for updates, translate coding rules into editing logic, and document edits for traceability.
remote, NY, United States$135k – $165k/yrFull TimeSenior (5+ years)Machinify
Source, design, validate, and maintain clinical and coding content for claims editing products. Monitor authoritative sources for updates, translate coding rules into editing logic, and document edits for traceability.
remote, United States$135k – $165k/yrFull TimeSenior (5+ years)
PSI CRO
Serve as the primary contact for medical and safety inquiries in clinical trials. Monitor participant safety, provide regulatory input, and develop trial-specific documents. Train trial teams, manage trial risks, and review safety reports and protocol deviations.
remote, United StatesFull TimeSenior (5+ years)
Word Monster
Write clear, accurate content for medical education and medical affairs deliverables, including slide decks and training materials. Deliver clinical trial materials and review content from writers, providing constructive feedback.
remote (anywhere)$61k – $75k/yrFull TimeSenior (5+ years)
Rho Inc
Provide medical, clinical, and scientific advisory expertise across therapeutic areas. Review trial-related Adverse Events and Serious Adverse Events, ensuring safety and integrity in clinical trials. Support project teams with medical input for clinical programs and regulatory guidance.
remote, United StatesFull TimeDirector10,000,000+ more jobs available!
