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Temporary Remote Medical Writing 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 ...

YO AI Labs

Medical Writer - Remote

Seattle, WA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Chicago, IL · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Phoenix, AZ · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

New York, NY · Remote

$50 - $80/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Palo Alto, CA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Austin, TX · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Atlanta, GA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Washington, DC · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Philadelphia, PA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Seattle, WA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Boston, MA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

San Francisco, CA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Miami, FL · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

San Jose, CA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Houston, TX · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Dallas, TX · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Los Angeles, CA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

YO AI Labs

Medical Writer - Remote

Boston, MA · Remote

$50 - $90/hr

Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 Guidelines * Scientific Accuracy Assessment * Source Data Verification * Clinical Protocol Interpretation * TFL Analysis ...

micro1 AI

Medical Writing Manager

Gilbert, AZ · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on developing advanced AI-assisted writing tools for clinical documentation. In ...

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Temporary Remote Medical Writing information

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$11

$46

$78

How much do temporary remote medical writing jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for temporary remote medical writing in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

What is the difference between Temporary Remote Medical Writing vs Temporary Remote Medical Editing?

AspectTemporary Remote Medical WritingTemporary Remote Medical Editing
Primary RoleCreating and developing medical content, such as clinical study reports, manuscripts, and regulatory documents.Reviewing, proofreading, and refining medical documents for clarity, accuracy, and compliance.
Required SkillsStrong writing, medical knowledge, and understanding of regulatory guidelines.Excellent editing skills, attention to detail, and medical terminology expertise.
Work EnvironmentRemote, often project-based with pharmaceutical or biotech companies.Remote, supporting medical writers or regulatory teams in document review.
Common CertificationsMedical degree or related certification, writing experience.Editing certification, medical background preferred.

Temporary Remote Medical Writing focuses on creating original medical content, while Temporary Remote Medical Editing involves reviewing and refining existing documents. Both roles require medical knowledge and often operate remotely within the pharmaceutical and biotech industries, but they differ in their core responsibilities and skill sets.

More about Temporary Remote Medical Writing jobs

What cities are hiring for Temporary Remote Medical Writing jobs?

Cities with the most Temporary Remote Medical Writing job openings:

What states have the most Temporary Remote Medical Writing jobs?

States with the most job openings for Temporary Remote Medical Writing jobs include:

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The top searched job categories for Temporary Remote Medical Writing jobs are:

Temporary Remote Medical Writing jobs near you
Infographic showing various Temporary Remote Medical Writing 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 $96,235 per year, or $46.3 per hour.

Medical Writer

Sigma Systems, Inc.

Marlborough, MA • Remote

Contractor

Posted 4 days ago

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