Title: Clinical Research Manager PMCF EU MDR
Company: Global Regulatory Writing and Consulting
Global is seeking candidates with EU Medical Device Regulation (MDR) knowledge to join our exciting Post Market Clinical Follow-Up (PMCF) Team who have knowledge of medical device clinical data requirements. Experience in developing regulatory strategy for international medical device studies is preferred.
To find additional details on this position, please visit https://globalrwc.com/job-posting---clinical-research-manager
SOCRA Exp: 10/15/2020