Medical Writer I/II
Parexel
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇨🇳 China
Visit company websiteJob Level
Mid-LevelSenior
Tech Stack
Google Cloud Platform
About the role
- Author Clinical Documents including informed consents, clinical study reports, and safety update reports.
- Review and revise document drafts based on team feedback while following SOPs and guidelines.
- Perform literature searches and reviews to support document development.
- Ensure high-quality deliverables and data integrity across documents.
- Serve as primary client contact for medical writing projects including negotiating timelines and resolving issues.
- Prepare documents for publishing readiness and supervise team members in project documentation.
Requirements
- Bachelor's degree in Life Sciences/Health Related Sciences or equivalent
- Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, e.g., ICH-GCP
- Extensive clinical/scientific writing skills
- Advanced word processing skills, including MS Office (expertise in Word)
- Fluent in written and spoken English with appropriate attention to phraseology, grammar, and punctuation.
- Scientific background essential; writing experience includes multiple clinical study reports.
Benefits
- Health insurance
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical writingdocument authoringliterature reviewdata integritypublishing readinessMS OfficeWord processingclinical study reportsinformed consentssafety update reports
Soft skills
communicationnegotiationteam collaborationattention to detailproblem-solving
Certifications
Bachelor's degree in Life SciencesBachelor's degree in Health Related Sciences