JOB DETAILS
Clinical Research Associate II
CompanyPSI CRO
LocationSaint-Maur-des-Fossés
Work ModeOn Site
PostedJune 10, 2026
About The Company
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas.
PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines.
PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world.
PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees.
http://www.psi-cro.com
About the Role
Company 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 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)
Key Skills
On-site MonitoringCRF ReviewSource Document VerificationQuery ResolutionSite ManagementStudy StartupFeasibility ResearchRegulatory DocumentationOncologyHemophiliaInfectious DiseasesGastrointestinalEnglish ProficiencyMS OfficeMultitaskingProblem-solving
Categories
Science & ResearchHealthcareConsulting
Benefits
Professional Advancement OpportunitiesMentorship And Training ProgramFlexible Working HoursHome-office OptionOnboarding TrainingsProfessional Development Training ProgramsPositive Team AtmosphereAdditional Leave Days (12 days of RTT)
Job Information
📋Core Responsibilities
The role involves conducting and reporting all types of onsite monitoring visits and managing site communications. Responsibilities include CRF review, source document verification, and supporting the regulatory team with study submissions.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
2891
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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