Clinical Research Associate II

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

📋 Description

• Conduct and document various onsite monitoring visits

• Participate in the initiation of studies

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

• Oversee communication and management at the site level

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

• Coordinate with internal project teams about the progress of studies

• Engage in feasibility assessments

• Assist the regulatory team in preparing documents for study submissions

• Enhance clinical research skills and broaden therapeutic area knowledge

⛳️ Requirements

• College/University degree in Life Sciences or a comparable mix of education, training, and experience

• Experience in independent on-site monitoring in France

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

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

• Full working proficiency 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 professional growth opportunities within Clinical Operations with dedicated mentorship and training programs

• Opportunities for development across various PSI departments

• Flexible working hours

• Option for remote work

• Hybrid work arrangement combining home and office

• Comprehensive onboarding and professional development training programs

• Well-established company culture and a supportive team environment

• Additional leave days (12 days of RTT)