Clinical Research Associate - Sponsor Dedicated - Turkey
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Turkey
Publicado em January 9, 2024
Detalhes do emprego
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What will you be doing?
- Help when requested, in preparation of regulatory submissions. Design of patient information sheets and consent forms. Ensure timely submission of protocol/consent documents for ethics/IRB approval.
- Pre study/placement and initiation visits.
- Conduct regular monitoring visits in accordance with the ICON site monitoring SOP/sponsor site monitoring SOP, as appropriate .
- Maintain all files and documentation pertaining to studies.
- Deal with sponsor generated queries in a timely manner. Ensure the satisfactory closeout of investigator sites and the correct archiving of files on completion of a study. Maintain patient and sponsor confidentiality. Assume additional responsibilities as directed by the Project Manager.
- Previous experience in a Clinical Research Associate role.
- Oncology experience
- Fluent in English
- G-Bachelor's Level Degree
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