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Pharmd Medical Writer Jobs (NOW HIRING)

MJH Life Sciences

Medical Writer

Washington, DC

$85K - $100K/yr

Medical Writer At MJH Life Sciences our success is measured by your success! If you set your ... Advanced degree (PhD, PharmD, MD, or equivalent) in a life science or medical discipline preferred;

IQVIA

Principal Medical Writer

Durham, NC

Bachelor's degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred * Minimum of 7+ years of experience in medical writing ...

IQVIA, Inc.

Principal Medical Writer

Durham, NC · On-site

Bachelor's degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred * Minimum of 7+ years of experience in medical writing ...

IQVIA LLC

Bachelor's degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred. * Minimum of 7+ years of experience in medical writing ...

MJH Life Sciences

Medical Writer

Washington, DC

$85K - $100K/yr

Medical Writer At MJH Life Sciences our success is measured by your success! If you set your ... Advanced degree (PhD, PharmD, MD, or equivalent) in a life science or medical discipline preferred;

Iambic Therapeutics, Inc

Principal Medical Writer

$152K - $190K/yr

Bachelor's degree in a life science (or health-related field) required; advanced degree (Masters/PhD/PharmD) preferred with a minimum 10 years of relevant medical writing experience * Demonstrated ...

Real Chemistry

Medical Writer

Boston, MA · On-site

D., MD, PharmD) preferred * 3 + years of experience in a Medical Communications agency setting ... Expert writing and editorial skills with medical terminology expertise * Strong verbal and written ...

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How much do pharmd medical writer jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for pharmd medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is a PharmD medical writer?

A PharmD Medical Writer is a professional with a Doctor of Pharmacy (PharmD) degree who specializes in creating scientific and medical content. They translate complex pharmaceutical and clinical information into clear and accurate documents for healthcare professionals, regulatory agencies, or the general public. Their work may include writing clinical study reports, regulatory submissions, drug monographs, medical education materials, and promotional content. Strong research skills, knowledge of medical terminology, and the ability to communicate complex information effectively are essential. These writers often work for pharmaceutical companies, medical communication agencies, or as freelancers.

What are the typical daily responsibilities of a PharmD medical writer?

As a PharmD Medical Writer, your typical day may involve drafting, editing, and reviewing a range of scientific documents, such as clinical study reports, regulatory submissions, and peer-reviewed manuscripts. You often collaborate with clinical teams, scientists, and regulatory affairs professionals to ensure scientific accuracy and clarity in all materials. Additionally, you may participate in literature reviews, data analysis, and respond to feedback from clients or subject matter experts. There is a strong emphasis on meeting deadlines and maintaining compliance with industry standards and guidelines throughout your writing projects.

What are the key skills and qualifications needed to thrive as a PharmD medical writer, and why are they important?

To thrive as a PharmD Medical Writer, you need a doctorate in pharmacy (PharmD), strong scientific writing skills, and deep knowledge of medical terminology and drug development. Familiarity with reference management software, publication guidelines (such as ICMJE, GPP), and regulatory documentation tools like Microsoft Word and EndNote is typically required. Exceptional attention to detail, time management, and effective communication skills help you stand out in this collaborative and fast-paced field. These skills are essential to ensure accuracy, compliance, and clarity in producing high-quality medical documents for various stakeholders.

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Pharmd Medical Writer jobs near you
Infographic showing various Pharmd Medical Writer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Medical Writer / Clinical Document - Remote

Chicago, IL • Remote

YO AI Labs
See more jobs at YO AI Labsexternal

$50 - $80/hr

Full-time

Re-posted 5 days ago

Job description

Job Title: Medical Writer / Clinical Document Author

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.