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Medical Writer Analyst Jobs (NOW HIRING)

YO AI Labs

Medical Writer - Remote

San Jose, CA · On-site

$50 - $80/hr

TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.

YO AI Labs

Medical Writer - Remote

Boston, MA · On-site

$50 - $80/hr

TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.

Veristat

Principal Medical Writer

England, AR · On-site +1

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... The primary responsibilities of the position are organizing, analyzing, interpreting, and ...

CSL

Principal Medical Writer

King Of Prussia, PA · On-site

... and for analyzing proposed plans, programs, individual studies and related documents for their ... Leads the Medical Writing contributions to assigned clinical Programs * Drives and develops the ...

New

Veristat

Principal Medical Writer

Columbia, SC · On-site +1

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... The primary responsibilities of the position are organizing, analyzing, interpreting, and ...

YO AI Labs

Medical Writer - Remote

Seattle, WA · Remote

$50 - $90/hr

TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.

YO AI Labs

Medical Writer - Remote

Chicago, IL · Remote

$50 - $90/hr

TFL Analysis * eCTD Knowledge * Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.

Veristat

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... The primary responsibilities of the position are organizing, analyzing, interpreting, and ...

Veristat

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... The primary responsibilities of the position are organizing, analyzing, interpreting, and ...

Veristat

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... The primary responsibilities of the position are organizing, analyzing, interpreting, and ...

IQVIA LLC

Principal Medical Writer

Durham, NC · On-site

Overview We are seeking an experienced Principal Medical Writer to lead the development of high ... Broad understanding of clinical research processes, including study design, data analysis, and ...

Veristat

Principal Medical Writer

Ontario, CA · On-site +1

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... The primary responsibilities of the position are organizing, analyzing, interpreting, and ...

CSL Plasma Inc.

The Principal Medical Writer is a key leadership position responsible for determining and driving ... Ability to analyze critically and synthesize complex scientific information from a range of ...

New

IQVIA

Principal Medical Writer

Durham, NC · On-site

Overview We are seeking an experienced Principal Medical Writer to lead the development of high ... Broad understanding of clinical research processes , including study design, data analysis, and ...

Veristat

Principal Medical Writer

Scotland, PA · On-site +1

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... The primary responsibilities of the position are organizing, analyzing, interpreting, and ...

IQVIA

Principal Medical Writer

Durham, NC · On-site

Overview We are seeking an experienced Principal Medical Writer to lead the development of high ... Broad understanding of clinical research processes , including study design, data analysis, and ...

IQVIA, Inc.

Principal Medical Writer

Durham, NC · On-site

Overview We are seeking an experienced Principal Medical Writer to lead the development of high ... Broad understanding of clinical research processes , including study design, data analysis, and ...

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Medical Writer Analyst information

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How much do medical writer analyst jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for medical writer analyst in the United States is $19.71, according to ZipRecruiter salary data. Most workers in this role earn between $13.70 and $19.95 per hour, depending on experience, location, and employer.

What is a medical writer analyst?

A Medical Writer Analyst is a professional who creates, reviews, and analyzes scientific documents related to medicine, healthcare, and clinical research. They translate complex medical information into clear, accurate, and regulatory-compliant documents for various audiences, such as healthcare professionals, regulatory authorities, and patients. Their work often includes clinical study reports, regulatory submissions, scientific manuscripts, and educational materials. Medical Writer Analysts also ensure that all documentation meets industry standards and guidelines. They play a crucial role in communicating scientific findings and supporting the drug development process.

What are the key skills and qualifications needed to thrive as a medical writer analyst?

To thrive as a Medical Writer Analyst, you need strong scientific knowledge, excellent writing skills, and a relevant degree in life sciences or a related field. Familiarity with medical writing software (such as EndNote or Reference Manager), document management systems, and understanding of regulatory guidelines (like ICH or FDA requirements) are typically required. Attention to detail, critical thinking, and the ability to communicate complex information clearly are essential soft skills. These competencies ensure the accurate translation of scientific data into clear, compliant documents that support regulatory submissions and medical communications.

How does a medical writer analyst typically collaborate with cross-functional teams during a project?

Medical Writer Analysts frequently work alongside clinical researchers, regulatory affairs specialists, and subject matter experts to ensure accuracy and compliance in documentation. They participate in project meetings to gather relevant data, clarify scientific concepts, and align on timelines. Effective communication skills are essential, as they often serve as the bridge between scientific teams and non-technical stakeholders. This collaborative environment helps ensure that all regulatory and publication documents meet both scientific and industry standards.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals or those with specialized skills can earn over $100,000 per year. Freelance medical writers may have variable income depending on project volume and client rates.

How can I get into medical writing with no experience?

Medical Writer Analysts often start by gaining a strong understanding of scientific and medical concepts through self-study, online courses, or certifications such as those from the American Medical Writers Association. Building a portfolio with sample writing, volunteering for related projects, and developing skills in scientific research, editing, and familiarity with tools like reference management software can help entry into the field without prior experience.

Is there a demand for medical writer analysts?

Medical writer analysts are in demand due to the growing need for clear, accurate scientific communication in healthcare, pharmaceuticals, and biotech industries. They often require strong writing skills, knowledge of medical terminology, and familiarity with regulatory guidelines, with employment opportunities available in pharmaceutical companies, research organizations, and medical communications agencies.

What cities are hiring for Medical Writer Analyst jobs?

Cities with the most Medical Writer Analyst job openings:

What states have the most Medical Writer Analyst jobs?

States with the most job openings for Medical Writer Analyst jobs include:

What are popular job titles related to Medical Writer Analyst jobs?

For Medical Writer Analyst jobs, the most frequently searched job titles are:

Infographic showing various Medical Writer Analyst job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $40,987 per year, or $19.7 per hour.

Medical Writer - Remote

San Jose, CA • On-site

YO AI Labs
See more jobs at YO AI Labsexternal

$50 - $80/hr

Other

Re-posted 2 days ago

Job description

Job Title: Medical Writer Expert Remote

Location: Remote
Job Type: Contractor
Pay: $50–$80/hour

Job Overview

We are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing.

Key Responsibilities

  • Author and review Clinical Study Reports (CSRs) and other regulatory documents.

  • Interpret clinical protocols and ensure compliance with ICH guidelines.

  • Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.

  • Review safety documentation, including DSURs and PSURs/PBRERs.

  • Provide structured feedback and collaborate with cross-functional teams.

  • Support AI-assisted documentation evaluation and quality improvement initiatives.

Required Skills

  • Regulatory Medical Writing

  • Clinical Study Report (CSR) Authoring

  • ICH E3 Guidelines

  • Scientific Accuracy Assessment

  • Source Data Verification

  • Clinical Protocol Interpretation

  • TFL Analysis

  • eCTD Knowledge

  • Strong Written Communication & Collaboration

Qualifications

  • 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.

  • Experience authoring Clinical Study Reports and regulatory documentation.

  • Strong knowledge of ICH E3, ICH E2F, ICH E2C, and eCTD requirements.

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

  • Experience in oncology and haematology is preferred.

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