Clinical Research Associate II

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

📋 Description

• Execute and document various onsite monitoring visits.

• Participate actively in the initiation of studies.

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

• Manage site communications and oversee site operations.

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

• Update internal project teams on the progress of studies.

• Engage in feasibility assessments.

• Assist the regulatory team in preparing materials for study submissions.

• Conduct clinical studies across various therapeutic areas while upholding high-quality standards.

⛳️ Requirements

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

• Proven independent on-site monitoring experience in France.

• Familiarity with all types of monitoring visits in Phase II and/or III trials.

• Background in oncology, hemophilia, infectious diseases, or gastrointestinal studies.

• Fluent in English with full working proficiency.

• Skilled in MS Office applications.

• Capable of planning, multitasking, and thriving in a fast-paced team environment.

• Strong communication, collaboration, and problem-solving abilities.

• Willingness to travel as needed.

• CV/resume must be provided in English.

🏝️ Benefits

• Significant professional growth opportunities within Clinical Operations, including tailored mentorship and training programs.

• Opportunities for development across various PSI departments.

• Flexible working hours to accommodate personal schedules.

• Option for remote work from home.

• Hybrid work arrangement combining both home and office settings.

• Comprehensive onboarding and professional development training programs.

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

• Additional leave days (12 days of RTT).