CRA I
About the role
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Job Field: Clinical Operations
Employment Status: Permanent
- You will work within a large-scale, fast-paced international environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate, monitor and close-out investigational sites for clinical studies in phases I to IV, ensuring adherence to applicable SOPs, regulations and principles of ICH-GCP.
- Data entry
- With a University degree in science or equivalent, you have a minimum of 6-12 months experience as a Clinical Research Associate on clinical studies, all possible therapeutic areas (preferred: TBD per country), in a CRO, Pharma industry or hospital environment.
- You have a driving license and are available to travel throughout France.
- Your dynamism, your autonomy, your relationship, your keen sense of organization and your willingness to deliver within required timelines and according to the desired quality, makes you ideally suited to evolve in this function.
- Fluent in English (written, read, spoken).
ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.
Application process
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