A leading global Contract Research Organization is seeking a Site Coordinator to manage study tasks at investigational sites. The role involves data entry, patient recruitment, and compliance with regulatory requirements under the supervision of a Principal Investigator. Ideal candidates should have a clinical science background, GCP certification, and familiarity with eCRF/EDC systems. Proficiency in Norwegian is mandatory. Join a team dedicated to improving patient lives and develop your career in a supportive environment.
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