Clinical Research Associate Ii - Sponsor Dedicated - Based In Netherlands
Syneos Health
Netherlands
Remote
On-site and remote monitoring
Ensure gcp compliance
Develop monitoring tools
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices
Job Summary
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates.
Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct.
Matching Summary
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
Skills & Requirements
Must-have
On-site and remote monitoring
Ensure GCP compliance
Develop monitoring tools
Collaborate with cross-functional teams
Fluency in Dutch
Nice-to-have
Drug development mindset
Agile and driven to deliver
Inclusive culture
Key Requirements
Bachelor's degree or equivalent experience
2-4 years of experience in clinical research monitoring