Language / 言語
At SunFlare, we form long-term partnerships
with experienced translators and interpreters.
This role involves preparing nonclinical documents (toxicology, pharmacology, and pharmacokinetics), including responses to regulatory inquiries.
![Medical Writer / Pharmaceuticals, Clinical Trials & Biotechnology [Clinical and Regulatory Documentation]](https://recruit.sunflare.com/jobs/storage/recruits/vZXLnHDTKn7BywWtIOlA5Ivk0teu3gTyzaL2rZLD.jpg)
Urgent Recruitment: Writer for “List of Prohibited Concomitant Medications” and “Clinical Trial Notification” Documents
This is a job posting for a medical writer responsible for preparing pharmacovigilance (PV) documents such as DSURs and periodic safety reports.
This job involves checking and proofreading translated documents in the pharmaceutical and clinical trial fields.
This role involves preparing CMC-related documents such as CTD Modules 2.3 and 3 for regulatory submissions, as well as responses to regulatory inquiries.
The deadline for downloading the application documents and trial assaignment file is within one week of submitting your application. As a general rule, the submission deadline is within 1 week of the date and time you download the trial file (this may vary by subject, e.g., within 24 hours). Please note that submission deadlines are strictly and automatically managed down to the exact date and time by the system, so be sure to submit well in advance. For details, please refer to the application guidelines.
No, applying and taking the trial are completely free of charge.
Yes, applicants living outside Japan are also eligible to apply.
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