Director, Medical Safety- Sponsor-Dedicated (m/w/d)

Frankfurt, Hesse, Germany Budapest, Hungary Sofia, Bulgaria Ljubljana – Dunajska, Slovenia Bucuresti, Romania Madrid, Spain Lisbon, Portugal Zaventem, Belgium Belgrade, Serbia Riga, Latvia Zagreb, Croatia Reading, Berkshire, United Kingdom Prague, Czech Republic Tallinn, Estonia Copenhagen, Denmark Full time R1558654 Responsibilities Conduct medical review of clinical trial and post-marketing safety data, including adverse events (AEs), adverse drug reactions (ADRs), coding, causality, expected…