Medical Writer II / メディカルライターII (在宅勤務可)
Parexel · Japan
Medical Writing
Remote
physician
Nurse
Pharmacist
Demand82
Career growth72
Healthcare fit70
Remote potential65
5-year outlook
Stable demand is likely for experienced bilingual medical writers in CROs and pharma, with progression toward senior medical writer, SME, or regional lead roles. Compensation should grow with document-type breadth and regulatory/submission experience, though exact pay is not stated in the posting.
Clinical license
Not required
Applicant reach
narrow
Seniority
mid
Employment type
full-time
Date found
2026-11-06
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Profession fit
- physician, Nurse, Pharmacist
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering for experienced medical writers or clinicians who already have CRO/pharma medical writing experience and strong Japanese-English skills. Most clinicians without a writing portfolio or regulatory document experience will find the experience bar too high for this specific role.
Who should apply
Bilingual Japanese-English medical writers with CRO or pharmaceutical experience; clinicians or pharmacists who have worked on clinical trial documents, regulatory submissions, safety reports, or medical publications; former clinical research or regulatory professionals seeking a medical writing career in a global CRO.
CV angle
Frame real clinical, research, or pharma experience around document authoring and regulatory communication: protocols, informed consent forms, clinical study reports, CTD modules, safety reports, publications, and cross-functional review. Emphasize Japanese-English bilingual communication, therapeutic-area knowledge, SOP adherence, and collaboration with medical, statistical, clinical operations, and regulatory teams without inventing writing experience.
Skills to highlight
- Medical writing
- CTD and regulatory submissions
- Clinical study reports and protocols
- Japanese-English bilingual communication
- Cross-functional collaboration
- SOP compliance and document quality
- Project coordination
Role summary
A mid-level medical writing role at Parexel Japan producing clinical and regulatory documents such as protocols, informed consent forms, clinical study reports, CTD sections, safety reports, manuscripts, and abstracts. The position works closely with clients and cross-functional teams and offers remote work flexibility and global medical writing team exposure.
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