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Wednesday 19 December 2018
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Rochester, New York
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This position supports the Cardiology Division as a research coordinator in pharmaceutical and device clinical trials. Typical duties will include but are not limited to: conducting study protocols as the primary coordinator, with responsibility for study start-up activities such as WIRB and RSRB submissions, recruitment and enrollment and entire conduct of given study under the direction of the Principal Investigator. Ensures compliance with all applicable regulatory and institutional requirements and standards as well as compliance with Good Clinical Practice (GCP) guidelines and sponsor requirements. On-call responsibilities are expected, dependent on individual study protocols. This position will assist the administrative efforts of the Manager/Senior Health Project Coordinator and Director of the Research to assess clinical feasibility of newly proposed projects, evaluating study protocols regarding standard of care and research-oriented tasks, evaluating time and effort needed to complete clinical tasks and study procedures and visits related to conducting of the studies toward assessment and preparation of budgets for the studies. This person will be committed to providing high-quality research efforts on the Cardiology Division's behalf.
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