Clinical Research

• Independently conduct and document onsite and remote monitoring activities, including site qualification, initiation, monitoring and close-out visits across Serbia and Croatia
• Ensure investigative sites comply with protocols, ICH-GCP, applicable regulations, SOPs and project requirements
• Act as primary contact for assigned sites and resolve questions, issues, action items and protocol deviations
• Review clinical trial data, source documentation and study systems for accuracy, completeness, data integrity and compliance
• Support site selection, activation, recruitment, study milestones and patient recruitment targets
• Train sites on protocols, study systems, processes and applicable requirements
• Maintain essential study documentation, including ISF and TMF
• Collaborate with sponsors, project teams, vendors and investigative sites
• Participate in audits, inspections, Investigator Meetings, study meetings and other project activities
• Mentor CRA I and II colleagues, participate in co-monitoring and CRA assessments, and contribute to process improvement

Explore Senior Clinical Research Associate, Serbia at Alimentiv. Review requirements and application details.

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