Language / 言語
At SunFlare, we form long-term partnerships
with experienced translators and interpreters.
This job involves checking and proofreading translated documents in the pharmaceutical and clinical trial fields.
This role involves preparing clinical regulatory documents related to pharmaceutical development, including CSRs, CTDs, study protocols, and responses to regulatory inquiries.
This role involves preparing pharmacovigilance (PV) documents, including DSURs, PBRERs, and other safety reports.
This role involves preparing nonclinical regulatory documents, including CTD nonclinical sections and documentation related to toxicology, pharmacology, and pharmacokinetics.
This role involves preparing CMC regulatory documents, including CTD Modules 2.3 and 3.
Japanese-English Communication Support Staff (Interpretation & Translation)
The deadline for downloading the application documents and trial assignment file is within one week of submitting your application. As a general rule, the submission deadline is within one 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.
Effective communication creates value.
Put your skills to work at SunFlare.
