Clinical Research Associate II/Senior CRA

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

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions

College/University degree in Life Sciences or an equivalent combination of education, training & experience

Independent on-site monitoring experience in France

Experience in all types of 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 plan, multitask and work in a dynamic team environment

Communication, collaboration, and problem-solving skills

Ability to travel

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

We offer:

• Big professional advancement opportunity within Clinical Operations with specific mentorship and training program
• Development opportunities across PSI departments
• Flexible working hours
• Home-office option available, as well as combination of home and office work arrangement
• Extensive onboarding trainings and professional development training programs
• Highly developed company culture and positive team atmosphere
• Additional leave days (12 days of RTT)