Regulatory Support Consultant - AWARD

CPI are looking for somebody that can work both independently and collaboratively with a consortium of partners to: • Engage with the MHRA (Scientific Advisory Meetings/Clinical Assessors). • Compile and report development and pre-clinical data for MHRA discussion/review. • Provide regulatory guidance on vaccine development, including but not limited to: - Use of preservatives - Specifications - Storage conditions - Shelf life - Adjuvant selection • Support with the design of Phase I clinical study. • Lead compilation of the IMPD

Prior experience in Phase I vaccines, liaising with the MHA and IMPD development would be essential.