One of the largest clinical development service providers in Japan
Job Overview
We are looking for a skilled Medical Writer to join our Clinical Data Science team at a global joint venture that combines the expertise of a top-tier global CRO and a well-known Japanese pharmaceutical service provider.
Key Responsibilities
Create clinical development documents such as protocols, informed consent forms, Investigator's Brochures, Clinical Study Reports (CSRs), and Common Technical Documents (CTDs).
Collaborate with internal teams and external vendors to oversee timelines and project progress.
Perform quality control (QC) checks on clinical documents.
Requirements
Must-Have:
• Minimum 3 years of medical writing experience at a pharmaceutical company or CRO.
• Experience in authoring CTD clinical modules is essential.
• TOEIC score of 600+ or equivalent English proficiency.
Work Location
Tokyo or Osaka
Working Hours & Benefits
• Core hours: 11:00 AM – 4:00 PM (Flex time: 7:30 AM – 8:00 PM)
• Standard Hours: 9:00 AM – 6:00 PM (8 hrs/day, 1 hr break)
• Annual holidays: 122 days (including weekends, public holidays, New Year)
• Paid leave: 10–20 days annually (granted after 3-month probation)
• Other leave: Summer, maternity, parental, bereavement, and caregiving leave
Compensation & Benefits:
• Commuting allowance (company policy)
• Overtime pay (unless hired as management)
• Retirement benefits (Defined Contribution Pension - 401K)
• Social insurance (health, pension, employment, and workers’ comp)
• Group insurance, congratulatory/condolence payments
• Access to member-only resorts, sports clubs (via Benefit One)
• Company housing (for transfers assigned by the company)