info الوصف
الوظيفي
Four (4) years clinical research experience with at least two (2) years of clinical monitoring experience or Master’s degree with 2 years clinical research experience.
Applied understanding of any applicable regulations (e.g., Good Clinical Practices, ICH guidelines, FDA CFR, ISO, clinical research ethics, HIPAA and patient privacy laws, EU Directive, etc.).
Business knowledge or experience with the medical / healthcare industry.
Class III medical device and/or phase II, III and IV pharmaceutical experience.
Experience to demonstrate understanding of technical, scientific and medical information.