Germany Browse · Frankfurt Am Main · Clinical Research Associate
Abbott
Benefits: attractive abbott pension plan, compyny ...
This role supports the advancement of heart disease treatment through breakthrough medical technologies in atrial fibrillation and Left Atrial Appendage Occlusion
IQVIA UK
Perform site selection, initiation, monitoring, and close-out visits in Germany and Switzerland
TFS HealthScience
The Clinical Research Associate (CRA) plays a key role in ensuring high‑quality clinical trial execution across all study phases
ICON Clinical Research, LP
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development
ICON Clinical Research, LP
As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies
ICON Clinical Research, LP
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
ICON Clinical Research, LP
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
ICON Clinical Research, LP
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
ICON Clinical Research, LP
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
ICON Clinical Research, LP
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
ICON Clinical Research, LP
As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies
ICON Clinical Research, LP
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities. Our success depends on the quality of our people, and we offer a range of benefits designed to support well-being and work-life balance
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization
IQVIA UK
Join IQVIA Biotech as a Clinical Research Associate 2 to work home-based throughout Germany
IQVIA UK
Join IQVIA as a Clinical Research Associate and work home-based throughout Germany
IQVIA UK
Join IQVIA as a Clinical Research Associate and work home-based throughout Germany
IQVIA
You will perform site selection, initiation, monitoring and close-out visits, and support the development of a subject recruitment plan
