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.

• Participate in the initiation of studies.

• Conduct CRF assessments, source document verification, and resolve queries.

• Manage communication and oversight at the site level.

• Serve as the primary contact for internal support services and vendors.

• Liaise with internal project teams regarding the progress of studies.

• Engage in feasibility assessments.

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

• Conduct clinical studies across a range of therapeutic areas while upholding high-quality standards.

⛳️ Requirements

• Bachelor's degree in Life Sciences or an equivalent 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 studies.

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

• Full professional proficiency in English.

• Competence in MS Office applications.

• Capacity to plan, multitask, and thrive in a dynamic team environment.

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

• Willingness to travel.

• Candidates are requested to submit their CV/resume in English.

🏝️ Benefits

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

• Opportunities for development across various PSI departments.

• Flexible working hours.

• Option for remote work available.

• Hybrid work arrangement combining home and office settings.

• Comprehensive onboarding training sessions.

• Access to professional development training programs.

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

• Additional leave days (12 days of RTT).