Remote Medical Writer: Regulatory & Clinical Submissions

Placements24; Myrtle Beach (SC); Remote; USD 55,000 - 96,000; Full time

Benefits offered by this job

Competitive hourly or project-based st

Remote contract role

Job summary

Placements24 is seeking a highly skilled Remote Medical Writer to support regulatory submissions, clinical trial reporting, and scientific communications in a fully remote, contract-based role. You will author, edit, and review complex documents, collaborating with cross-functional teams to ensure accuracy and adherence to ICH, FDA, and EMA guidelines.

The ideal candidate has 4+ years of medical writing experience in pharma/biotech/CRO settings, strong writing skills, and the ability to work

Qualifications

• Bachelor's or Master's degree in scientific/healthcare field.
• PhD is a plus for advanced regulatory roles.
• Minimum 4 years as a Medical Writer in pharma/biotech/CRO.

Responsibilities

• Author, edit, and review medical/regulatory documents (protocols, IBs, CSRs, CTD modules, manuscripts).
• Ensure documents meet ICH, FDA, EMA guidelines and are scientifically sound.

Skills

Medical writing

Regulatory documentation

Attention to detail

Remote work management

Education

Bachelor's or Master's degree in Life Sciences/Healthcare

PhD considered a plus

Tools

Microsoft Word

Adobe Acrobat

Document management systems

Job description

Placements24 is seeking a highly skilled Remote Medical Writer to support regulatory submissions, clinical trial reporting, and scientific communications in a fully remote, contract-based role. You will author, edit, and review complex documents, collaborating with cross-functional teams to ensure accuracy and adherence to ICH, FDA, and EMA guidelines.

The ideal candidate has 4+ years of medical writing experience in pharma/biotech/CRO settings, strong writing skills, and the ability to work