About this role
Country Approval Specialist / Regulatory Officer at PSI CRO. Location: Ra'anana, Central District, Israel. Role: preparing submissions, communicating regulators, managing reporting Requirements: Prepare clinical trial submission dossiers, communicate with authorities and ethics committees, review submission documents and translations, track regulatory documentation, manage safety reporting, and deliver regulatory training. Requires 1+ year Israel clinical submissions experience. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Office, Matarot Commitment: Full Time Workplace: Onsite Languages: English, Hebrew