Clinical Research Associate I/II

• Monitor and own the progress of clinical studies at investigative sites
• Ensure clinical studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, and applicable regulations and standards
• Coordinate activities required to set up and monitor studies
• Identify investigators
• Help prepare regulatory submissions
• Conduct pre-study and initiation visits
• Travel to sites for monitoring visits
• Identify potential study risks and propose mitigation solutions
• Prepare for investigator meetings, site visits, and project team updates
• Handle study-related difficulties and conflicts
• Take responsibility for the quality and outcomes of work

• Based in Paris or the Paris area, France
• Life science degree and/or equivalent experience
• 1 year or more as a CRA in a CRO or pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies
• Site management or equivalent experience in clinical research
• Experience managing oncology studies
• Availability for domestic travel including overnight stays, up to approximately 50–60% travel commitment
• Excellent communication and organizational skills
• Team-player capability
• Evidence of a client-focused approach
• Fluency in English and, for non-English-speaking countries, the local language of the country where the position is based
• Candidates must be legally authorized to work in the country of employment without employer sponsorship
• Please apply in English

• Lower than average number of protocols
• Reasonable travel and improved work/life balance
• Direct line management support
• Growth support
• Remote-based work arrangement
• Equal Opportunity Employer
• Reasonable accommodation support for applicants with disabilities