Cancer Clinical Trials Regulatory Specialist

Beth Israel Deaconess Medical Center (BIDMC) is seeking a Regulatory Affairs professional to support cancer center trials and regulatory submissions within the Cancer Clinical Trials Office (CCTO). The role involves preparing IRB submissions, amendments, INDs, and safety reports, and liaising with the IRB to resolve queries.

The ideal candidate has a life science degree with 1–3 years in regulatory affairs, and familiarity with FDA and NIH guidelines.