Manager, Regulatory Affairs-hybrid role
Adaptimmune
- Abingdon, Oxfordshire
- Permanent
- Full-time
- Contributes to the development of the global regulatory strategy and executes regulatory strategies for assigned projects
- Preparation of regulatory submissions including: INDs, CTAs, GMOs, IDEs, amendments, annual reports, meeting briefing documents, responses to regulatory agency information requests, marketing authorization applications, and other regulatory submissions, as applicable.
- Serves as the primary liaison with FDA and other regulatory agencies throughout development of projects, including support for regulatory agency meetings and teleconferences
- Identify and assess existing and new regulations, guidance documents, international standards, or consensus standards; and provide interpretive guidance and ensure applicable implementation into development planning and execution
- Ensures that all regulatory activities and documents to be submitted to regulatory agencies have been evaluated to assure that they are complete, well organized, scientifically accurate, of high quality, are in regulatory compliance to facilitate agency review and acceptance
- Represents Global Regulatory Affairs as a member of the cross-functional project team, providing regulatory guidance/strategy/perspective in team meetings
- Reviews and establishes standard operating procedures (SOPs) and global regulatory affairs processes
- Ensure regulatory documentation is maintained appropriately
- Other duties as assigned
- Bachelor’s Degree required; advanced degree preferred
- Experience in drug development process
- Minimum 3 years of Regulatory Affairs experience
- Must have experience filing regulatory dossiers (CTAs, INDs, IMPDs, IDEs)
- Solid working knowledge of relevant domestic and global regulations and guidance
- Experience in cell and gene therapy and/or oncology is strongly preferred
- Experience with BLAs/NDAs/MAAs preferred