Clinical Research Associate II

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.

• Carry out CRF assessments, source document verification, and resolve queries.

• Manage and facilitate communication with site personnel.

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

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

• Engage in feasibility studies.

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

• Contribute to clinical studies spanning various therapeutic areas while upholding high-quality standards.

⛳️ Requirements

• A college or university 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 during Phase II and/or III.

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

• Full working proficiency in English.

• Competency in MS Office applications.

• Capability to plan, multitask, and thrive in a dynamic team setting.

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

• Willingness to travel.

• CV/resume must be provided in English.

🏝️ Benefits

• Significant opportunities for professional advancement within Clinical Operations, including a tailored mentorship and training program.

• Opportunities for development across various PSI departments.

• Flexible working hours.

• Home-office options available.

• A blend of remote and office-based work arrangements.

• 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).