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Clinical Research Associate II

PSI CRO

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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.

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

Benefits

  • Big professional advancement opportunity within Clinical Operations with specific mentorship and training program

Development opportunities across PSI 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) Please submit your CV/resume in English
  • 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.