About the role
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 * Your CV/resume must be submitted in English
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) * Please submit your CV/resume in English