As Director Site Management & Monitoring, you will play a key role in steering and developing clinical study activities with strategic responsibility and international collaboration
Job Summary
As Director Site Management & Monitoring, you will play a key role in steering and developing clinical study activities with strategic responsibility and international collaboration.
You will lead and develop Clinical Research Associates and other monitoring roles, ensuring clinical studies are conducted with high quality, compliance, and patient safety.
Pfizer is committed to inclusion and equal opportunity, encouraging applicants to bring their best with the assurance of reasonable accommodations.
Matching Summary
As Director Site Management & Monitoring, you will play a key role in steering and developing clinical study activities with strategic responsibility and international collaboration.
Skills & Requirements
Must-have
Site Management & Monitoring
Clinical Study Quality and Compliance
Leadership of Clinical Research Associates
Stakeholder Management
Strategic Clinical Trial Oversight
GCP and Regulatory Compliance
Nice-to-have
Coaching and Employee Development
International Collaboration
Process Improvement and Innovation
Virtual/Remote Monitoring Approaches
Representation in External Networks
Key Requirements
Completed degree in natural sciences, medicine, or pharmacy
Extensive experience in clinical research
Experience in international pharma or CRO environment