Clinical Research Associate II

Psi CRO; Saint-Maur-des-Fossés; Hybrid; EUR 42,000 - 65,000; Full time

Benefits offered by this job

Home-office option

Hybrid work arrangement

Professional development

Job summary

PSI is seeking a Clinical Research Associate to perform onsite monitoring across diverse therapeutic areas in France, participate in study startup, and support regulatory submissions. You will manage site communications, coordinate with vendors, and liaise with internal teams to track study progress.

English proficiency and willingness to travel are required. The role offers a home-office option and a hybrid work arrangement in a dynamic Clinical Operations environment with mentorship and

Qualifications

• College/University degree in Life Sciences or equivalent.
• Independent on-site monitoring experience in France.
• Experience in monitoring visits in Phase II/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.
• Strong communication, collaboration and problem-solving skills.
• Ability to travel.

Responsibilities

• 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.

Skills

Independent on-site monitoring

Monitors Phase II/III visits

Oncology, hemophilia, infectiousDiseas

English proficiency

MS Office

Planning & multitasking

Communication & collaboration

Travel ability

Education

Life Sciences degree

Tools

MS Office

Job description

PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

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

Qualifications

• 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

Additional Information

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 acrossPSI departments
• 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)

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