Clinical Research Associate Ii And Senior Clinical Research Associate
Clinchoice
Germany, Germany
On-site
Medical device monitoring
Gcp/ich guidelines knowledge
Site performance oversight
As a CRA, you’ll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices
Job Summary
As a CRA, you’ll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices.
You will oversee site performance, conduct company-initiated clinical studies, and ensure high-quality deliverables through site visits, monitoring, and effective communication.
Join a dynamic, global team that values growth, collaboration, and making a difference in clinical research.
Matching Summary
As a CRA, you’ll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices.
Skills & Requirements
Must-have
medical device monitoring
GCP/ICH Guidelines knowledge
site performance oversight
clinical study management
Nice-to-have
direct sponsor partnership
global reach and stability
career development opportunities
Key Requirements
Fluent in German
Fluent in English
Bachelor's Degree or equivalent
Up to 8 years of experience as a CRA
At least 4 plus years of onsite monitoring experience
Previous medical device monitoring experience
Therapeutic area experience in neuro- or cardiovascular domain