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Medical Writer Editor Jobs (NOW HIRING)

Merican

Medical Writer

Medical Writer Location: Paramus, NJ, 07652 Job Type: Temporary Assignment Duration: 5 Months Work ... Excellent scientific writing, editing, and document structuring skills * Ability to simplify ...

Applied Underwriters

Writer/Editor

Omaha, NE

Proficiency in Associated Press writing style; and understanding of SEO, GEO and UX writing best practices Our Benefits Include: * 100% employer-paid medical, dental, and vision insurance for ...

Applied Underwriters

Writer/Editor

Omaha, NE · On-site

Proficiency in Associated Press writing style; and understanding of SEO, GEO and UX writing best practices Our Benefits Include: * 100% employer-paid medical, dental, and vision insurance for ...

Telix Pharmaceuticals (AMER)

OR

Lead the compilation, writing, and editing of high-quality regulatory documents and reports ... Understanding medical terminology and statistical methodology is a must. * Experience writing ...

Lumanity

Senior Medical Writer

Yardley, PA · Remote

Outstanding writing, editing and communication skills and excellent command of the English language ... Medical, dental, and vision insurance options * 401(k) plan with employer match * Generous amount ...

DR Horton, Inc.

Content Writer/Editor-Temp *

Austin, TX · On-site

R. Horton, Inc. is currently looking for a Content Writer/Editor for their Marketing Department ... We offer an excellent benefits package including vision, medical and dental. Build YOUR future with ...

Lumanity

Senior Medical Writer

Yardley, PA · On-site +1

Outstanding writing, editing and communication skills and excellent command of the English language ... Medical, dental, and vision insurance options * 401(k) plan with employer match * Generous amount ...

Lumanity

Senior Medical Writer

Yardley, PA · Remote

Outstanding writing, editing and communication skills and excellent command of the English language ... Medical, dental, and vision insurance options * 401(k) plan with employer match * Generous amount ...

Calyx

Medical Writer

Provide medical editing review of draft and final documents prepared by other medical writers before internal or external distribution. This includes both copyediting and content review. * Follow ...

Node.Digital

Technical Writer & Editor

Arlington, VA · On-site

Technical Writer & Editor Location: Arlington, VA Must have an active Top Secret Clearance Must be ... Medical * Dental * Vision * Basic Life * Health Saving Account * 401K * Three weeks of PTO * 10 ...

INTECON

Technical Writer / Editor

Scott Air Force Base, IL · On-site

$70K - $90K/yr

Job Role: Technical Writer / Editor - MAF Mission Planning Systems LCAT: Technical Support ... Comprehensive Group Health Plans (Medical, Dental, and Vision) coverage. * Company-paid Short-Term ...

iHeartMedia, Inc.

News Writer/Editor

Phoenix, AZ · On-site

What We Need: We are looking for a strong news writer/editor with sharp journalism skills. The ... Employer sponsored medical, dental and vision with a variety of coverage options * Company provided ...

TRI Challenge Convention

Medical Writer

Bethesda, MD · Hybrid

Superior writing skills that require moderate to minimal editing. Knowledge of regulatory ... Ability to analyze medical research data and review experimental protocols. Meets expectations with ...

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Medical Writer Editor information

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$37K

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How much do medical writer editor jobs pay per year?

As of Jul 21, 2026, the average yearly pay for medical writer editor in the United States is $84,537.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,000.00 and $101,500.00 per year, depending on experience, location, and employer.

How do Medical Writer Editors typically collaborate with clinical teams and subject matter experts during the document development process?

Medical Writer Editors work closely with clinical teams, researchers, and subject matter experts to ensure scientific accuracy and clarity in documents such as clinical study reports, manuscripts, and regulatory submissions. They often participate in meetings, conduct interviews, and review data with these professionals to gather necessary information and resolve ambiguities. This collaboration helps maintain compliance with regulatory standards and ensures the content is both scientifically sound and accessible to the target audience. Effective communication and strong interpersonal skills are essential for success in this aspect of the role.

What is the difference between Medical Writer Editor vs Medical Writer?

AspectMedical Writer EditorMedical Writer
CredentialsTypically requires a degree in life sciences or related field; editing certifications are a plusUsually holds a degree in life sciences, communications, or journalism; writing certifications are common
Work EnvironmentEditorial teams, publishing houses, pharmaceutical companiesResearch institutions, healthcare companies, pharmaceutical firms
Employer & Industry UsageUsed in publishing, regulatory writing, and medical communicationsUsed in clinical research, medical marketing, and regulatory submissions

Medical Writer Editors focus on refining and editing medical content for clarity, accuracy, and compliance, often combining writing skills with editing expertise. Medical Writers primarily create original medical content, including research papers, regulatory documents, and marketing materials. While both roles require strong scientific knowledge, the key difference lies in editing versus content creation.

What is a Medical Writer Editor?

A Medical Writer Editor is a professional who creates, reviews, and edits scientific documents related to medicine and healthcare. They ensure that complex medical information is presented accurately, clearly, and in compliance with regulatory guidelines. Their work may include writing clinical study reports, regulatory submission documents, journal articles, and educational materials. Medical Writer Editors also check for grammar, consistency, and adherence to formatting standards, making the content suitable for its intended audience.

What are the key skills and qualifications needed to thrive as a Medical Writer Editor, and why are they important?

To thrive as a Medical Writer Editor, you need a solid background in life sciences or medicine, excellent writing and editing abilities, and familiarity with scientific literature. Proficiency with reference management software, document formatting tools, and industry-specific style guides (such as AMA or ICMJE), as well as certifications like the Medical Writer Certified (MWC), are often required. Strong attention to detail, project management skills, and the ability to convey complex information clearly are crucial soft skills in this role. These competencies ensure the creation of accurate, compliant, and accessible medical content for diverse audiences.
More about Medical Writer Editor jobs
What cities are hiring for Medical Writer Editor jobs? Cities with the most Medical Writer Editor job openings:
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Medical Writer Editor jobs near you
Infographic showing various Medical Writer Editor job openings in the United States as of July 2026, with employment types broken down into 53% Locum Tenens, 35% Full Time, 10% Part Time, and 2% Contract. Highlights an 71% Physical, 5% Hybrid, and 24% Remote job distribution, with an average salary of $84,537 per year, or $40.6 per hour.
Medical Writer

Medical Writer

Merican

Remote

Other

Re-posted 23 days ago

Job description

Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.
Job Title: Medical Writer
Location: Paramus, NJ, 07652
Job Type: Temporary Assignment
Duration: 5 Months
Work Type: Remote
Shift: Mon-Fri 9.00 AM-5.00 PM
Job Description:
  • We are seeking a skilled Medical Writer to develop high-quality clinical and regulatory documents in compliance with industry standards and regulatory guidelines.
  • The ideal candidate will collaborate with cross-functional teams, including Clinical, Regulatory, Biostatistics, and Medical Affairs, to create well-structured, scientifically accurate, and regulatory-compliant documents.

DUTIES AND RESPONSIBILITIES
Regulatory Document Writing:
  • Prepare and author clinical and regulatory documents, including but not limited to:
  • Clinical Study Protocols (CSPs) and Protocol Amendments
  • Clinical Study Reports (CSRs)
  • Investigator's Brochures (IBs)
  • Informed Consent Forms (ICFs)
  • Common Technical Document (CTD) Modules (e.g., Module 2.5 Clinical Overview, Module 2.7 Clinical Summary)
  • Briefing Documents for Regulatory Authorities (e.g., FDA, EMA)
  • Periodic Safety Reports
  • Risk Management Plans (RMPs) and Pediatric Investigation Plans (PIPs)
  • New Drug Applications (NDAs), Biologics License Applications (BLAs), and Marketing Authorization Applications (MAAs)
  • Responses to regulatory queries

Clinical Development Support:
  • Develop and maintain clinical development plans, clinical trial protocols, and statistical analysis plans
  • Collaborate with clinical teams to ensure alignment of clinical documents with study objectives and regulatory requirements
  • Interpret complex scientific and clinical data and communicate findings clearly and concisely
  • Regulatory Compliance & Standards:
  • Ensure documents comply with ICH, GCP, FDA, EMA, and other applicable regulatory agency guidelines
  • Maintain up-to-date knowledge of regulatory writing best practices, industry trends, and evolving guideline

Collaboration & Review:
  • Work closely with cross-functional teams, including medical, clinical, regulatory, statistical, and quality assurance teams
  • Review and edit documents prepared by internal teams or external vendors to ensure scientific accuracy, clarity, and compliance
  • Participate in team meetings, regulatory interactions, and strategy discussions
  • Drive document production timelines according to established plans
  • Plan and manage multiple simultaneous document development projects with shifting priorities

EDUCATION PREFERRED :
  • Advanced degree (PhD, PharmD, MD, or MSc) in Life Sciences, Medicine, Pharmacy, or a related field

WORK EXPERIENCE:
  • Minimum 3-5 years of medical writing experience in the pharmaceutical, biotech, or CRO industry
  • Strong background in writing regulatory documents for clinical trials and submissions
  • Epilepsy or Neurology experience is a plus
  • Experience with drug development across different phases (Phase I-IV) is a plus
  • Strong understanding of the drug development process, clinical research concepts, clinical study conduct, clinical study data collection, regulatory requirements, and biostatistical concepts
  • Familiarity with medical terminology and ability to interpret complex clinical data
  • Strong understanding of the concepts of coding dictionaries (MedDRA, WHODrug, etc.)
  • Excellent scientific writing, editing, and document structuring skills
  • Ability to simplify complex scientific concepts for diverse audiences
  • Proficiency in ICH guidelines, GCP, and regulatory submission requirements (FDA, EMA, etc.)
  • Strong attention to detail, ability to manage multiple projects, and meet deadlines
  • Ability to work independently and collaboratively in a fast-paced environment
  • High level of Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
  • Experience with document management systems and publishing tools (e.g., EndNote, Adobe Acrobat, regulatory submission platforms)
  • Veeva experience

PHYSICAL AND MENTAL REQUIREMENTS
  • Ability to multitask
  • Maintain composure under pressure
  • Ability to follow verbal or written instructions and use of effective verbal communications
  • Adapts and adjusts to change and grasps information quickly
  • Detail-oriented

OTHER:
  • Must have excellent, concise, and clear written and oral communication skills; possess strong analytical and interpersonal skills, ability to work independently.
  • Highly motivated self-starter witha a positive attitude, possessing the initiative required to achieve desired goals both independently and within a team structure.
  • Demonstrated project management ability.
  • Excellent interpersonal, oral and written communication skills.
  • Strong relationship-building skills.
  • Team-oriented, with the ability to work effectively with others

TekWissen® Group is an equal opportunity employer supporting workforce diversity.
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About Merican

Sourced by ZipRecruiter

Merican is a IT Service consulting firm, specialized in Digital adoption and Business automation. With our diverse collection of skilled and committed consultants, technology companies, businesses and digital experts, we provide our subject expertise and our unique client service approach, a best-in-class global model of delivery suited to the business demands of our clients. We ensure that we implement future-oriented solutions for our clients via investments in people, solutions, technologies, competencies and infrastructure.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Columbia , MD, US

Year founded

2020

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