Clinical Research Associate
Posted Oct 26
Posted Oct 26
This is a fully remote position, open to applicants in Greece.
• Execute site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure adherence to protocols, data integrity, and patient safety throughout the trial phases.
• Collaborate with investigators and site personnel to ensure seamless study execution.
• Conduct data review and resolve queries to uphold high-quality clinical data standards.
• Assist in the preparation and evaluation of study documentation, including protocols and clinical study reports.
• Assume responsibility for clinical trial monitoring deliverables and work in a cooperative manner.
• Bachelor's degree in a scientific or healthcare-related discipline.
• A minimum of 2 years of experience as a Clinical Research Associate.
• Comprehensive knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Excellent organizational and communication skills, with a keen attention to detail.
• Capability to work independently as well as collaboratively in a fast-paced environment.
• Willingness to travel as needed (approximately 60%).
• Legal authorization to work in the country where the position is located.
• Competitive base salary along with performance-related incentives.
• Health and wellness programs, including medical, dental, and vision coverage where applicable.
• Retirement and pension schemes.
• Life insurance and disability coverage.
• Employee assistance programs and wellness resources.
• Opportunities for learning and development through structured training and career pathways.
Alphanumeric Systems
ICON plc
ICON plc
ICON plc
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