The University of Minnesota's Masonic Cancer Center Clinical Trials Office is seeking a Regulatory Manager to oversee regulatory submissions and documentation for clinical studies. The role emphasizes compliance with FDA and GCP regulations, IRB interactions, and audit readiness, with a strong focus on collaboration with investigators and study teams.
Hybrid/remote work is available with required in-person dates.
#J-18808-LjbffrRemote Regulatory Specialist, Clinical Trials in workfromhome at Unknown Company
This position is listed as full time and able to be worked remotely.