About this role
Startup Associate at Fortrea. Location: Tokyo, Tokyo, Japan. Role: collecting documents, compiling submissions, liaising vendors Requirements: 0–2+ years clinical research or regulatory experience; university/college degree (life science preferred) or equivalent experience; working knowledge of ICH/GCP, IRB/IEC/RA submissions; ability to collect, quality‑review, compile and track regulatory documents. Category: Research and Development (R&D) Seniority: Entry Level Tools: Clinical Trials Information System (CTIS) Commitment: Full Time Workplace: Hybrid Languages: English