Our client will run a small safety study for 48 participants but need their brief protocol reviewed and potentially drafted. They currently are working on the protocol but need assistance with a Gap assessment and support to complete the protocol.
This project would be a review of the protocol for safety studies – phase 1; cannabinoids and infusion delivered therapies. We are looking for someone with regulatory and medical writing expertise.
If you are interested in this role, please send your resume and explanation of your experience to Consultingjobs@Advarra.com