Clinical Research Associate II - Remote & Growth

Psicro; France; Hybrid; EUR 42,000 - 60,000; Full time

Benefits offered by this job

Big professional advancement within CL

Mentorship and training program

Flexible working hours

Home-office option

Onboarding trainings and development

Positive team atmosphere

Additional RTT leave

Job summary

PSI is seeking a Clinical Research Associate to conduct onsite monitoring visits and support study startup across diverse indications. You will ensure high-quality data through CRF reviews, source data verification, and query resolution while maintaining effective site communications.

Ideal candidates hold a Life Sciences degree and have independent on-site monitoring experience in France, with Phase II/III exposure, English proficiency, and strong MS Office skills.

Qualifications

• College/University degree in Life Sciences or equivalent.
• Independent on-site monitoring experience in France.
• Experience in monitoring visits in Phase II and/or III.
• Experience in oncology, hemophilia, infectious diseases, GI.
• Full working proficiency in English.
• Proficiency in MS Office applications.
• Ability to travel.
• Communication, collaboration and problem-solving skills.

Responsibilities

• Conduct and report onsite monitoring visits.
• Be involved in study startup and feasibility research.
• Perform CRF review, source data verification and query resolution.
• Manage site communications and vendor interactions.
• Coordinate with in-house teams on study progress.
• Support regulatory documents for submissions.
• Plan, multitask and work in a dynamic team.

Skills

On-site monitoring

Study startup

CRF review

Vendor coordination

Communication

Multitasking

Travel readiness

Education

Life Sciences degree

Tools

MS Office

Job description

PSI is seeking a Clinical Research Associate to conduct onsite monitoring visits and support study startup across diverse indications. You will ensure high-quality data through CRF reviews, source data verification, and query resolution while maintaining effective site communications.

Ideal candidates hold a Life Sciences degree and have independent on-site monitoring experience in France, with Phase II/III exposure, English proficiency, and strong MS Office skills.