Clinical Research Associate II

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

📋 Description

• Perform and document various onsite monitoring visits.

• Participate in the initiation of studies.

• Conduct CRF review, verify source documents, and resolve queries.

• Manage communication and oversight of site operations.

• Act as a liaison for internal support services and vendors.

• Update internal project teams on study developments.

• Engage in feasibility assessments.

• Assist the regulatory team with the preparation of study submission documents.

• Contribute to clinical studies across diverse therapeutic areas while ensuring high-quality standards.

⛳️ Requirements

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

• Proven independent on-site monitoring experience in France.

• Familiarity with all types of monitoring visits for Phase II and/or III studies.

• Experience in oncology, hemophilia, infectious diseases, and gastrointestinal conditions.

• Fluent in English with full working proficiency.

• Proficient in MS Office applications.

• Strong planning, multitasking, and teamwork abilities in a dynamic environment.

• Excellent communication, collaboration, and problem-solving skills.

• Willingness to travel as needed.

• 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 working hours.

• Option for remote work.

• Hybrid work arrangement combining home and office settings.

• Comprehensive onboarding and professional development training programs.

• A well-established company culture and a positive team environment.

• Additional leave days (12 days of RTT).