In this role, you will have strategic responsibility for site management and monitoring activities in Germany, ensuring clinical studies are conducted with high quality, compliance, and efficiency
Job Summary
In this role, you will have strategic responsibility for site management and monitoring activities in Germany, ensuring clinical studies are conducted with high quality, compliance, and efficiency.
You will lead and develop Clinical Research Associates and other monitoring roles, contributing to the growth and evolution of the team and clinical study environment.
Pfizer is committed to inclusion and equal opportunity, encouraging applicants to bring their best selves with the assurance of reasonable accommodations throughout the application and career.
Matching Summary
In this role, you will have strategic responsibility for site management and monitoring activities in Germany, ensuring clinical studies are conducted with high quality, compliance, and efficiency.
Skills & Requirements
Must-have
Site Management and Monitoring
Clinical Study Quality and Compliance
Leadership of Clinical Research Associates
Stakeholder Management
Strategic Clinical Trial Oversight
GCP and Regulatory Compliance
Nice-to-have
Process Improvement Initiatives
Virtual and Remote Monitoring Approaches
International Collaboration
Coaching and Staff Development
Risk Management
External Representation and Networking
Key Requirements
Degree in natural sciences, medicine, or pharmacy
Extensive clinical research experience
Experience in international pharma or CRO environment
Leadership experience
Fluent German and very good English
Knowledge of clinical trial processes and regulations