Clinical Research Associate II

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

📋 Description

• Perform and document all varieties of onsite monitoring visits

• Engage in the initiation of studies

• Conduct CRF assessments, verify source documents, and resolve queries

• Manage site communication and oversight

• Serve as a liaison for in-house support services and vendors

• Update internal project teams on study advancements

• Contribute to feasibility studies

• Assist the regulatory team in preparing documents for study submissions

• Participate in clinical studies across various therapeutic areas while upholding high quality standards

⛳️ Requirements

• Bachelor's degree in Life Sciences or a comparable mix of education, training, and experience

• Independent onsite monitoring experience in France

• Experience conducting all types of monitoring visits in Phase II and/or III

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

• Proficient in English

• Skilled in MS Office applications

• Capable of planning, multitasking, and thriving in a dynamic team setting

• Strong communication, collaboration, and problem-solving abilities

• Willingness to travel

• CV/resume must be submitted in English

🏝️ Benefits

• Significant opportunities for professional growth within Clinical Operations, including a dedicated mentorship and training program

• Opportunities for development across various PSI departments

• Flexible work hours

• Option for remote work

• Hybrid work arrangement combining home and office

• Comprehensive onboarding and professional development training programs

• Strong company culture and a positive team environment

• Additional leave days (12 days of RTT)