Job Description
Dormont Manufacturing Co is seeking a Clinical Monitor to oversee site qualification, initiation, and ongoing monitoring for regulatory compliance. Responsibilities include ensuring informed consent, data integrity, and IP handling, with on-site or remote support.
The role requires strong communication, document review, and travel up to 75% to various sites, with emphasis on GCP/ICH guidelines and collaboration with study teams.
#J-18808-Ljbffr