Clinical Research Associate II

Benefits

Additional Information

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

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Company Intel

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