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Remote Regulatory Medical Writer Jobs (NOW HIRING)

Veristat

... range of regulatory documents and medical communications to support all phases of product ... Remote working * Flexible time off * Paid holidays * Medical insurance * Tuition reimbursement

Veristat

... range of regulatory documents and medical communications to support all phases of product ... Remote working * Flexible time off * Paid holidays * Medical insurance * Tuition reimbursement

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

... regulatory documentation activities within a leading biotechnology environment. This fully remote ... Medical Writing ───── Requirements ───── Bachelor's degree or higher in a ...

Veristat

... range of regulatory documents and medical communications to support all phases of product ... Remote working * Flexible time off * Paid holidays * Medical insurance * Tuition reimbursement

Veristat

Senior Medical Writer

England, AR · Remote

... range of regulatory documents and medical communications to support all phases of product ... Remote working * Flexible time off * Paid holidays * Medical insurance * Tuition reimbursement

Veristat

... range of regulatory documents and medical communications to support all phases of product ... Remote working * Flexible time off * Paid holidays * Medical insurance * Tuition reimbursement

Merican

Medical Writer

Remote Shift: Mon-Fri 9.00 AM-5.00 PM * We are seeking a skilled Medical Writer to develop high-quality clinical and regulatory documents in compliance with industry standards and regulatory ...

Jj

Medical Writer III

Raritan, NJ · On-site +1

Remote work options may be considered on a case-by-case basis and if approved by the company ... Writing or coordinating clinical and regulatory documents such as, but not limited to, CSRs, IBs ...

Jj

Medical Writer III

Spring House, PA · On-site +1

Remote work options may be considered on a case-by-case basis and if approved by the company ... Writing or coordinating clinical and regulatory documents such as, but not limited to, CSRs, IBs ...

Calyx

Medical Writer

Follow required standard operating procedures (SOPs), templates, guidelines, regulations, client ... Non-English language (written and verbal) - desirable This role is remote. Candidates located in ...

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

As of Jul 18, 2026, the average hourly pay for remote regulatory 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 Regulatory Medical Writer vs Remote Medical Writer?

AspectRemote Regulatory Medical WriterRemote Medical Writer
CredentialsMedical degree, regulatory writing experience, certifications (e.g., RAC)Medical, scientific, or related degree; writing experience
Work EnvironmentPharmaceutical/biotech companies, CROs, regulatory agenciesPharmaceutical, biotech, healthcare, or scientific organizations
Industry UsageRegulatory submissions, INDs, NDAs, safety reportsResearch publications, clinical trial documentation, scientific publications
Search/Comparison IntentRegulatory documentation, compliance, submission writingScientific writing, research, publication

The main difference is that Remote Regulatory Medical Writers focus on preparing regulatory documents for drug approvals and compliance, often requiring specific regulatory knowledge and certifications. Remote Medical Writers have a broader scope, including scientific publications and research documentation. Both roles require strong writing skills and relevant scientific backgrounds, but Regulatory Medical Writers specialize in regulatory submissions and compliance processes.

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What cities are hiring for Remote Regulatory Medical Writer jobs? Cities with the most Remote Regulatory Medical Writer job openings:
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Remote Regulatory Medical Writer jobs near you
Infographic showing various Remote Regulatory Medical Writer job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.
Senior Regulatory Medical Writer - Fractional (Remote)

Senior Regulatory Medical Writer - Fractional (Remote)

Penfield Search Partners

Fairfield, CT • Remote

Other

Re-posted 2 days ago

Job description

Job Description Contact: Alexandra Spink - aspink@penfieldsearch.com No 3rd party candidates We are seeking a Senior Regulatory Medical Writer to provide fractional, on-demand support for regulatory submission activities. This role focuses on independently updating and finalizing regulatory documents to support ongoing agency interactions and submission deliverables, working alongside internal and contract writers. Scope of Work Independently update, revise, and finalize regulatory documents, including protocol and IB Support preparation and maintenance of protocol amendments, submission support documents, and related deliverables within Common Technical Document (CTD Modules 2-5) across the submission lifecycle (responses, amendments, briefing packages) Ensure scientific accuracy, clarity, consistency, and compliance across all regulatory documents Collaborate with internal teams and contract writers to ensure timely delivery aligned with regulatory and quality standards Support intermittent workload demands (~10-15 hours/week during active project periods) Qualifications Regulatory medical writing experience supporting IND, CTA, NDA, and/or BLA submissions Strong familiarity with Common Technical Document (CTD) structure and regulatory submission lifecycle (e.g., responses, amendments, briefing packages) Ability to work independently with minimal oversight in a fast-paced, cross-functional environment Strong attention to detail with demonstrated ability to ensure scientific and regulatory quality standards Proven collaboration experience with regulatory, clinical, and medical writing teams

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