Medical Writer I

Parexel

Medical Writer I at Parexel authoring and managing clinical documents in drug development. Ensuring quality and compliance with regulatory standards while collaborating with project teams.

Posted 6/19/2026full-timeShenyang • 🇨🇳 ChinaMid-LevelSeniorWebsite

About the role

Key responsibilities & impact

Author Clinical Documents including model informed consents and clinical study reports
Ensure document quality and adherence to regulatory guidelines
Manage medical writing projects and client communications
Provide medical editing review of documents
Attend and complete training as required

Requirements

What you’ll need

Bachelor's degree in Life Sciences/Health Related Sciences or equivalent
Demonstrated understanding of clinical research and the drug development process
Good clinical/scientific writing skills
Writing experience of regulatory documents
Good word processing skills, including MS Office (proficiency in Word)
Fluent in written and spoken English

Benefits

Comp & perks

Health insurance
Professional development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical writingregulatory document writingmedical editingdocument quality assuranceproject managementclinical research understandingdrug development process knowledgeword processingMS Officeproficiency in Word

Soft Skills

client communicationattention to detailtraining completionwritten communicationverbal communication

Certifications

Bachelor's degree in Life SciencesBachelor's degree in Health Related Sciences