Senior clinical research associate
SligoCollins McNicholas
...study sites Prepare and present site initiation & device training sessionsKnowledge, Skills and Experience Required for the Role: Strong knowledge of QMS, GCP & GLP for medical devices and clinical studies Understanding of Class III device regulations in EU, US & globally (ISO 14155 & EU MDR 2017/745) 5+ years’ experience in [...]
Category Science & Biotech
30+ days ago in Collins McNicholas