Experienced Clinical Research Associate, ICON Biotech
Core
Managing clinical studies for Small and Medium sized Biotech sponsors in the Netherlands, ensuring compliance with ICH-GCP and regulatory requirements across Phase I–III trials.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial delivery for biotech clients
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial monitoring, site qualification, regulatory submissions, study documentation management, cross-functional collaboration, issue resolution
Preferred skills
Proficiency with clinical trial systems and tools
Technologies
Clinical trial systems and tools
Responsibilities
Independently monitor Phase I–III clinical trials; Conduct site qualification, initiation, monitoring, and close-out visits; Manage study documentation, regulatory submissions, and ethics/IRB approvals; Ensure study cost efficiency and timely issue resolution
Seniority
Mid-level, hands-on IC