ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Clinical Research Associate
Location
France
Posted
7 days ago
Salary
0
Seniority
Mid Level
Job Description
Clinical Research Associate
ICON plc
• Contributing to clinical trial monitoring activities, taking responsibility for deliverables and working collaboratively • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process • Collaborating with investigators and site staff to facilitate smooth study conduct • Performing data review and resolution of queries to maintain high-quality clinical data • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
Job Requirements
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- 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 as required (approximately 60%)
Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- 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
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