About this role
About the Role ICON Biotech is seeking a Clinical Research Associate II (CRA II) to monitor and support Phase I–III clinical trials across multiple therapeutic areas in France. The role offers residency in Paris or Lyon with hybrid or remote work options, contributing to compliance, data integrity, and study execution within a dynamic biotech environment. What You'll Do
- Independently monitor Phase I–III clinical trials to ensure compliance with ICH-GCP and regulatory requirements
- Manage clinical studies in France across multiple therapeutic areas including Oncology (solid tumor and hematology/Car T cell), NASH, Neurology, Psychiatry, Cardiology and Dermatology
- Conduct site qualification, initiation, monitoring, and close-out visits
- 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
- Manage study documentation, regulatory submissions, and ethics/IRB approvals
- Ensure study cost efficiency and timely issue resolution What We're Looking For
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements within a CRO environment
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
- Fluency in French and professional proficiency in English
- Strong organizational and communication skills, with attention to detail Nice to Have
- Experience across multiple therapeutic areas including Oncology, NASH, Neurology, Psychiatry, Cardiology, Dermatology
- Familiarity with regulatory submissions and ethics/IRB processes in France
- Experience with trial budgeting and cost management Compensation & Benefits
- Competitive salary
- Various annual leave entitlements
- A range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 professionals for well-being support
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
- Visit our careers site to read more about the benefits ICON offers.