Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Parexel

Medical Writer II

Parexel

Medical Writer II at Parexel authoring and reviewing clinical documents for regulatory submissions. Ensuring quality and compliance while managing client communication and project timelines.

Posted 7/14/2026full-timeShanghai • 🇨🇳 ChinaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical writing and regulatory submissions, ensuring document quality and adherence to guidelines while effectively managing client communications and project timelines.

Highest-signal resume keywords
Clinical WritingRegulatory SubmissionDocument Quality AssuranceMS Office ExpertiseClinical Research Understanding

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical WritingRegulatory SubmissionDocument ReviewWord ProcessingClinical Research Knowledge
Soft Skills
Interpersonal CommunicationVerbal CommunicationWritten CommunicationTeam CollaborationProblem Mediation
Tools & Technologies
MS OfficeWord
Industry Keywords
Life SciencesHealth Related SciencesDrug Development Process

About the role

Key responsibilities & impact
  • Author clinical documents for regulatory submission
  • Ensure document quality and adherence to guidelines
  • Serve as primary client contact for medical writing projects
  • Review and revise documents based on team feedback
  • Manage timelines and mediate project-related issues

Requirements

What you’ll need
  • Bachelor's degree in Life Sciences/Health Related Sciences or equivalent
  • Excellent interpersonal, verbal, and written communication skills
  • Demonstrated understanding of clinical research and the drug development process
  • Extensive clinical/scientific writing skills
  • Advanced word processing skills, including MS Office (expertise in Word)
  • Fluent in written and spoken English

Benefits

Comp & perks
  • Health insurance
  • Professional development opportunities