Our client is a mid-sized global, specialty pharmaceutical company based in Princeton, NJ. They seek a Medical Writing professional with at least 5 years regulatory writing experience within the pharmaceutical industry, including managing global registration dossiers, to serve as a Senior Manager representative on a modality-specific International Medical Working Group. This person will manage the activities of internal/external resources and medical writing vendors (ie, individual consultant medical writers and contract research organization (CRO) medical writers), as well as prepare clinical documents as required (eg, Clinical Trial Reports, Periodic Safety Update Reports, clinical sections of IND/NDA/CTD).
Total compensation potential will reach 150K.
Stephanie Cousounis
Research Associate, Life Sciences,
Digital Action Inc.
StephanieC@digital-action.com
(610)941-0700 ext.102
Tags:
Share
-
▶ Reply to This