Clinical Research Associate II / Senior CRA

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

📋 Description

• Execute and document various types of onsite monitoring visits.

• Engage in the initiation of studies.

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

• Manage site communications and oversee site operations.

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

• Update internal project teams on the progress of studies.

• Contribute to feasibility studies.

• 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.

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

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

• Full working proficiency in English.

• Competence in MS Office applications.

• Strong planning, multitasking, and ability to thrive in a dynamic team environment.

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

• Willingness to travel.

• Please submit your CV/resume in English.

🏝️ Benefits

• Significant professional growth opportunities within Clinical Operations, featuring targeted mentorship and training programs.

• Opportunities for development across various PSI departments.

• Flexible working hours.

• Options for home-office arrangements, including a hybrid of remote and on-site work.

• Comprehensive onboarding training and ongoing professional development programs.

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

• Additional leave days (12 days of RTT).