Editor II, Consent Form Development

The Editor II, Consent Form Development role supports the IRB Services department by reviewing incoming submissions and preparing informed consent forms for human subject research. This position ensures regulatory compliance with FDA, HHS, Health Canada, TCPS2 regulations, and ICH GCP guidance while editing documents to align with organizational standards. The role involves collaborating with stakeholders, maintaining knowledge of human subject protection guidelines, and attending IRB meetings to enhance understanding of processes.