Clinical Research Associate Ii Or Senior Clinical Research Associate
Clinchoice
Belgium, Belgium
On-site
Medical device monitoring
Gcp/ich guidelines knowledge
Fluent in english and dutch
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
Fluent in English and Dutch
Site performance oversight
Clinical study management
Nice-to-have
Global reach and stability
Career development opportunities
Collaboration and growth focus
Key Requirements
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