Medical Writer I

Parexel

Medical Writer I at Parexel, responsible for authoring regulatory clinical documents and serving as client contact. Ensuring high-quality submissions while managing document-related project activities.

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

About the role

Key responsibilities & impact

Author clinical documents for submission to regulatory authorities
Gather, review, analyze, and evaluate resources for clinical document preparation
Ensure work is complete and of high quality before team distribution
Serve as primary client contact for medical writing projects
Attend and complete mandatory training

Requirements

What you’ll need

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
Good clinical/scientific writing skills
Writing experience of regulatory documents such as patient narratives, informed consent forms or similar
Good word processing skills, including MS Office (proficiency in Word)

Benefits

Comp & perks

Health benefits
Professional development opportunities

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 & Tools

clinical writingregulatory document preparationpatient narratives writinginformed consent forms writingclinical research understandingdrug development process knowledgeindustry guidelines knowledgeword processing skillsMS Office proficiencyscientific writing

Soft Skills

attention to detailquality assuranceclient communicationteam collaborationanalytical skills

Certifications

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