Clinical Research Associate II / Senior CRA

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions
• Work on clinical studies across different therapeutic indications while maintaining high quality standards

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Independent on-site monitoring experience in France
• Experience in all types of monitoring visits in Phase II and/or III
• Experience in oncology, hemophilia, infectious diseases, GI
• Full working proficiency in English
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel
• Please submit your CV/resume in English

• Big professional advancement opportunity within Clinical Operations with specific mentorship and training program
• Development opportunities across PSI departments
• Flexible working hours
• Home-office option available
• Combination of home and office work arrangement
• Extensive onboarding trainings
• Professional development training programs
• Highly developed company culture and positive team atmosphere
• Additional leave days (12 days of RTT)