Project Manager Clinical Studies
KI-Beschreibung
In this role, you will oversee complex clinical studies, ensuring they meet timelines and budgets while maintaining compliance with high-quality standards. You will coordinate with various stakeholders, manage submissions, and create essential project documentation.
Anforderungen
3–6 Jahre- •Degree in life sciences or equivalent combination of education, training and work experience in clinical trials
- •At least 3 years of experience as a Clinical Project Manager or 5-6 years as Clinical Research Associate at a CRO
/ medical device or pharmaceutical company - •Good knowledge of current industry practices related to the conduct of clinical studies