Clinical Research Associate II

This is a fully remote position, open to applicants in France.

📋 Description

• Execute and document all varieties of onsite monitoring visits

• Participate in the initiation of the study

• Conduct CRF evaluations, source document verification, and resolve queries

• Manage communication and oversight of site operations

• Serve as the key contact for in-house support services and vendors

• Liaise with internal project teams regarding the progress of the study

• Engage in feasibility assessments

• Assist the regulatory team in preparing documents for study submissions

⛳️ Requirements

• Bachelor’s degree in Life Sciences or a relevant combination of education, training, and experience

• Proven independent on-site monitoring experience in France

• Experience with various types of monitoring visits in Phase II and/or III

• Background in oncology, hemophilia, infectious diseases, and gastrointestinal studies

• Full working proficiency in English

• Competence in MS Office applications

• Capability to plan, prioritize, and function effectively in a dynamic team environment

• Strong communication, collaboration, and problem-solving abilities

• Willingness to travel

🏝️ Benefits

• Significant professional growth opportunities within Clinical Operations, supported by a dedicated mentorship and training program

• Opportunities for development across various PSI departments

• Flexible working hours

• Option for remote work, as well as a hybrid arrangement of home and office work

• Comprehensive onboarding training and professional development programs

• A well-established company culture with a positive team environment

• Additional leave days (12 days of RTT)