About this role
Regulatory Officer at PSI CRO. Location: Tokyo or Osaka or Japan. Role: preparing dossiers, tracking documentation, communicating stakeholders Requirements: University degree in life sciences/medicine/pharmacy, experience with PMDA clinical trial submissions, regulatory knowledge for clinical research, full working proficiency in English and Japanese, detail-oriented with strong communication skills. Category: Research and Development (R&D) Seniority: Entry Level Commitment: Full Time Workplace: Hybrid Languages: English, Japanese