Clinical Research Associate II/Senior CRA

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
Please submit your CV/resume in English

Employment type
Full-time

Work arrangement
Yes