Description:
Previous experience implementing, helping and managing medical device trials Significant knowledge of clinical and/or outcomes research study design Proven experience in protocol and ICF development, writing clinical section(s) for regulatory submission Proven experience in conducting literature searches, reviews and appraisal of the scientific data Excellent ability to interact with physicians and other professionals inside and outside the company Knowledge of Good Clinical Practice ICH/Google
May 1, 2025;
from:
dice.com