Celerion is seeking a Medical Writer to work remotely. The role analyzes and interprets safety results from clinical trials, compiling, writing and editing clinical study reports and other industry documents.
It requires accurate classification of events and medications using standardized coding systems. Responsibilities include drafting phase I/II documents, QC of safety text, and leading multi-disciplinary scientific reports while ensuring compliance with GCP/ICH and client specifications.
#J-18808-LjbffrRemote Medical Writer for Phase I/II Clinical Reports in Remote at Unknown Company
This position is listed as full time and able to be worked remotely.