Clinical Research Associate I

Job Listing No: 9740000

Clinical Research Associate I

Covance – Philippines – Primary responsibilities of a Clinical Research Associate: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned Responsible for all aspects of site management as prescribed in the project plans Recruitment of potential investigators, submissions preparation, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs Independently perform Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data … – Permanent – Full-time

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