14 set - Bardi
Icon Clinical
OverviewAs a Clinical Research Associate at ICON, you contribute to the design, analysis, and oversight of clinical trials to advance innovative therapies.
You will work closely with investigators and site staff to ensure study quality, patient safety, and regulatory compliance.
The role involves on-site monitoring, data review, and documentation as part of a collaborative team.
You will travel and operate in a fast-paced environment, driving trial integrity and timely delivery of study milestones.
Retribuzione / BenefitsCompetitive base salary and performance-related incentives
Health and wellbeing programmes including medical, dental, and vision coverage
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
ResponsabilitàConduct site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolution of queries to maintain high-quality clinical data
Contribute to preparation and review of study documentation, including protocols and clinical study reports
Requisiti fondamentaliBachelor's degree in a scientific or healthcare-related field
Minimum 2 years of experience as a Clinical Research Associate after certification as per Italian Law
Prior experience in Oncology Trials
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Willingness to travel approximately 60%
strong organizational skills
excellent communication
attention to detail
clinical trial processes knowledge
ICH-GCP guidelines
data review and query resolution
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