As Director Site Management & Monitoring, you will have strategic responsibility for clinical study site management and monitoring activities in Germany, ensuring high quality and regulatory compliance
Job Summary
As Director Site Management & Monitoring, you will have strategic responsibility for clinical study site management and monitoring activities in Germany, ensuring high quality and regulatory compliance.
You will lead and develop Clinical Research Associates and other monitoring roles while collaborating closely with internal and external partners to advance clinical research processes.
Pfizer is committed to inclusion and equal opportunity, providing an environment where employees can fully apply and develop their skills.
Matching Summary
As Director Site Management & Monitoring, you will have strategic responsibility for clinical study site management and monitoring activities in Germany, ensuring high quality and regulatory compliance.
Skills & Requirements
Must-have
Site Management & Monitoring in clinical trials
Quality, compliance and patient safety assurance
Leadership of Clinical Research Associates
Collaboration with global and local stakeholders
Strategic clinical study process development
Nice-to-have
Coaching and development of team members
Experience with virtual/remote monitoring approaches
Stakeholder management and communication skills
Strategic thinking and decision-making
Willingness to travel occasionally
Key Requirements
Completed degree in natural sciences, medicine, or pharmacy
Extensive experience in clinical research in international pharma or CRO environment
Leadership experience and passion for employee development