About this role
Regulatory Affairs CMC Associate II at Iovance Biotherapeutics. Location: United States. Role: manage submissions, prepare documents, maintain trackers Requirements: BS degree required; advanced degree preferred; minimum 5 years in regulatory affairs; experience with regulatory submissions (eCTD) for drug/biologic development. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Office Suite, Adobe Acrobat Pro Commitment: Full Time Workplace: Remote Languages: English