Medical Writer II
- Writing types
- Regulatory, Publications
- Seniority
- Mid
About the role
Responsibilities
- Prepare and edit clinical documents such as protocols, informed consent forms, CSRs and CTD sections
- Prepare safety reports including DSUR and PBRER, plus publications and abstracts
- Work with medical, statistical, clinical operations and regulatory teams on writing projects
Requirements
- 5+ years in the pharmaceutical industry and 3+ years as a medical writer
- Hands-on experience with CTD, clinical study reports and protocols
- Strong Japanese and English written and verbal communication
Preferred Qualifications
- Publication writing experience
- Experience facilitating meetings in English
About the Company
Parexel is a global clinical research organization with a dedicated medical writing services group serving clients worldwide.
Listed via Career sites