About this role
Regulatory Officer at PSI CRO. Location: Shanghai or Beijing. Role: procure documents, prepare dossiers, track progress Requirements: Bachelor's or higher in Medicine, Pharmacy, or Life Sciences; 5+ years in clinical trial submissions in China; English and Mandarin; MS Office; detail-oriented; team oriented. Category: Research and Development (R&D) Seniority: Mid Level Tools: MS Office, Regulatory submission software Commitment: Full Time Workplace: Onsite Languages: English, Chinese