Medical Writer (Pharmaceutical) (Remote) | $30–60/Hour
A medical writer (pharmaceutical) remote job is available for experienced regulatory medical writers and clinical document authors. This contractor opportunity involves reviewing clinical documentation, evaluating AI-generated content, and applying expert judgment to pharmaceutical writing tasks.
The project is particularly suited to professionals with substantial regulatory writing experience, including Clinical Study Reports and periodic safety documentation.
PROJECT DETAILS
This remote project focuses on developing AI-assisted tools for clinical documentation. Selected medical writers will create and evaluate realistic regulatory writing tasks while checking scientific accuracy, document structure, source support, and compliance with established clinical writing conventions.
The role is fully remote, with 30 openings available. For professionals exploring similar opportunities, browse more remote WFA jobs and relevant medical writing jobs on RemoteWFAJobs.
JOB INFORMATION
- Responsibilities: Author and review evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents; assess AI-generated regulatory content; verify narrative claims against tables, figures, listings, protocols, and source records; provide structured written feedback; and collaborate on evaluation frameworks and best practices.
- Qualifications: At least 5 years of regulatory medical writing experience at a sponsor, CRO, or independently; direct experience authoring or leading complete Clinical Study Reports; experience interpreting TFLs and protocols; and strong written and verbal communication skills.
- Technical Skills: ICH E3, ICH E2F, ICH E2C, eCTD knowledge, Clinical Study Report authoring, source data verification, clinical protocol interpretation, TFL analysis, scientific accuracy assessment, and AI-assisted documentation evaluation.
- Domain Expertise: Experience across multiple clinical phases and therapeutic areas is preferred, with oncology and haematology expertise especially valued.
- Education: An advanced degree in life sciences, pharmacy, or medicine, including PhD, PharmD, MD, or MSc, or equivalent depth of authoring experience.
- Contract Type: Contractor.
- Location: Remote.
COMPENSATION
The compensation range for this medical writer (pharmaceutical) remote job is $30–$60 per hour. The opportunity has 30 openings. Payment frequency and specific payment method are not provided in the available job details.
WHO SHOULD APPLY
This opportunity is designed for experienced pharmaceutical medical writers who can independently work with regulatory clinical documents and critically assess scientific content. Candidates should be comfortable tracing written claims back to clinical source data and distinguishing substantive scientific issues from acceptable stylistic variation.
Professionals with oncology or haematology experience and strong knowledge of ICH regulatory documentation may be especially aligned with the project requirements.
HOW TO APPLY
- Review the qualifications and technical requirements for the medical writing project.
- Prepare your professional information and relevant regulatory medical writing experience.
- Submit your application through APPLY HERE.
FAQ
What experience is required for this medical writer (pharmaceutical) remote job?
Candidates should have at least 5 years of regulatory medical writing experience and direct experience authoring or leading complete Clinical Study Reports.
Does this role require AI experience?
No prior AI experience is required. The project emphasizes pharmaceutical and regulatory writing expertise for evaluating AI-assisted clinical documentation.
Is oncology or haematology experience required?
It is not stated as mandatory, but oncology and haematology expertise is specifically valued among candidates.
CLOSING
Experienced regulatory medical writers can use this remote project to apply their clinical documentation expertise to AI-assisted writing evaluation. The role emphasizes scientific accuracy, regulatory structure, source verification, and practical medical writing judgment.
For more opportunities, explore the latest work-from-anywhere jobs and browse additional roles through the relevant job category on RemoteWFAJobs.
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