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Remote Pharmd Medical Writer Jobs (NOW HIRING)

Sigma Systems, Inc.

Medical Writer

Marlborough, MA · Remote

37554294 Remote Medical Writer, 7 Months Contract Sigma Systems is currently looking for a Remote Medical Writer The Medical Writer is responsible for authoring, reviewing, and coordinating the ...

Real Chemistry

Medical Writer

$75K - $85K/yr

Advanced degree (eg, MD, PhD, PharmD) required * Up to 1 year of previous medical writing experience in a medical communications agency preferred, but not essential * Familiarity with FDA, AMA and ...

Veristat

  • Medical

  • Retirement

Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... PhD, MD or PharmD preferred; science-related field preferred. * Minimum of 7 years of medical ...

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Remote Pharmd Medical Writer information

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$14

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How much do remote pharmd medical writer jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for remote 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 the difference between Remote Pharmd Medical Writer vs Remote Pharmd Medical Reviewer?

AspectRemote Pharmd Medical WriterRemote Pharmd Medical Reviewer
CredentialsPharmD, medical writing experience, possibly certifications in medical writingPharmD, strong review experience, familiarity with clinical data
Work EnvironmentRemote, primarily writing and creating scientific documentsRemote, focused on reviewing and editing medical content
Employer & IndustryPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, regulatory agencies, CROs

The main difference is that Remote Pharmd Medical Writers focus on creating scientific and regulatory documents, while Remote Pharmd Medical Reviewers concentrate on evaluating and editing existing medical content. Both roles require a PharmD and industry experience, but their daily tasks and responsibilities differ significantly.

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Remote Pharmd Medical Writer jobs near you
Infographic showing various Remote Pharmd Medical Writer 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 $80,364 per year, or $38.6 per hour.

Medical Writer

Sigma Systems, Inc.

Marlborough, MA • Remote

Contractor

This job post has expired today. Applications are no longer accepted.

Job description

37554294 Remote Medical Writer, 7 Months Contract
Sigma Systems is currently looking for a Remote Medical Writer
The Medical Writer is responsible for authoring, reviewing, and coordinating the development of high-quality clinical and regulatory documents that support global clinical development programs. This role works closely with cross-functional stakeholders to ensure documents are scientifically accurate, strategically aligned, and delivered according to established timelines and medical writing plans

Responsibilities:

  • Author, edit, and review clinical and regulatory documents, including:
    • Clinical study protocols and protocol amendments
    • Investigator Brochures (IBs)
    • Clinical Study Reports (CSRs)
    • Briefing Book support
    • IND and NDA summary documents and other regulatory submission materials
  • Develop documents that are consistent with regulatory requirements, internal standards, and medical writing plans, while supporting the overall clinical development lifecycle and program objectives for one or more clinical development programs.
  • Collaborate with cross-functional teams, including Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and Medical Affairs, to gather, interpret, and integrate scientific and clinical information into clear, accurate, and submission-ready documents.
  • Negotiate document deliverable milestones and timelines with cross-functional teams to ensure alignment across functions and adherence to medical writing plans and program objectives.
  • Facilitate document review cycles, resolve reviewer comments, and drive consensus among stakeholders while maintaining quality and schedule commitments.
  • Ensure documentation complies with applicable regulatory guidance, Good Clinical Practice (GCP), company standards, and industry best practices.
  • Contribute to the development and continuous improvement of medical writing processes, templates, style guides, and operational procedures.
  • Support regulatory submissions, health authority interactions, and inspection readiness activities as needed

Core Competencies

  • Scientific and regulatory writing expertise
  • Project and timeline management
  • Cross-functional collaboration and influence
  • Strategic thinking and problem solving
  • Attention to quality and regulatory compliance
  • Effective communication and stakeholder management

Requirements:

  • Advanced degree Bachelor's degree or more.
  • Experience authoring clinical and regulatory documents within the pharmaceutical, biotechnology, or clinical research industry.
  • Strong knowledge of clinical development, regulatory requirements, and applicable guidance documents (e.g., ICH guidelines).
  • Excellent scientific writing, editing, and communication skills.
  • Demonstrated ability to manage multiple projects and negotiate timelines in a cross-functional environment.

Strong organizational skills, attention to detail, and ability to work independently and collaboratively