Clinical Research Associate I - Sponsor dedicated - Netherlands - Home based (m/w/d)
Core
Conduct site qualification, initiation, monitoring, and close-out visits to ensure patient safety, data integrity, and protocol compliance across clinical trials.
Role type
Junior Clinical Research Associate (Sponsor-dedicated)
Builds
Clinical research programs for pharmaceutical and biotechnology sponsors
Domain
Life Sciences / Clinical Research
Required skills
GCP, ICH guidelines, site monitoring, patient recruitment, regulatory documentation, risk management
Preferred skills
Sponsor-dedicated or cFSP environment experience, patient recruitment and study start-up knowledge
Technologies
Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), Trial Master Files (TMF)
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits; Ensure investigational sites maintain high standards of patient safety and data integrity; Build and maintain effective relationships with investigators; Monitor study progress and resolve data queries; Collaborate on patient recruitment strategies; Maintain accurate study documentation; Identify and escalate study risks; Mentor junior team members.
Seniority
Junior, hands-on IC
