About this role
Regulatory Writer I at Ora. Location: United States. Role: authoring submissions, editing documents, tracking milestones Requirements: Master's in applied/life science or communications required; 1+ year medical/regulatory/clinical writing experience; ability to author and edit FDA and ex-US regulatory submissions (eCTD), interpret clinical data, and manage timelines. Category: Research and Development (R&D) Seniority: Entry Level Tools: eCTD Commitment: Full Time Workplace: Remote Languages: English