Germany onlyAs Director of Site Management & Monitoring, you will shape clinical research with global impact and play a key role in the management and development of our clinical study activities. You will be responsible for site management and monitoring activities in Germany and ensure that clinical studies are of high quality, compliant, and efficiently conducted.
Requirements
- Completed studies (e.g., natural sciences, medicine, pharmacy) or comparable qualifications
- Long-term experience in clinical research, preferably in an international pharmaceutical or CRO environment
- Leadership experience and enjoyment in developing staff is desirable
- Very good understanding of clinical study processes, monitoring, quality, and regulatory requirements
- Fluent German and very good English skills
- Excellent communication and stakeholder management skills
- Strategic thinking, decision-making, and a high level of self-responsibility
- Willingness to travel occasionally
United States
AU, CA + 6 more
India only
Georgia only