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Research FieldComputer science » Computer systemsEducation LevelUndergraduate Skills/Qualifications FURTHER Training in life sciences EXPERIENCE Support and support in the conduct of clinical trials
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of patient and monitor schedules. o Monitoring of the quality system o Participation in the medication management process. o Participation in the preparation and shipment of clinical trial patient samples. o
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administration, test performance, sample shipment, etc. o Supervision of the information systems of the clinical trials. o Supervision of the information systems used in the clinical trials. Requirements Research
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or equivalent Skills/Qualifications TRAINING Office automation advanced user level. EXPERIENCE Experience and knowledge in clinical trials. Experience in CRDe management and queries resolution. Database
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administrative support to the clinical trial team. Preparing and assisting monitors with materials required for visits. Maintain complete documentation of all trials to ensure complete and correct management
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the execution of clinical trials and their quality control: -Participation in the medication management process. -Preparation and shipment of clinical trial patient samples -Support in the monitoring
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, Project’s Main Researcher Pilar Alonso Lecue, Clinical Trials Coordinator of the Pneumology Service Galo Peralta, IDIVAL´s Management Director Patricia Álvarez-Ingelmo, IDIVAL Human Resources
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Degree or equivalent Skills/Qualifications Experience in clinical trials English Specific Requirements Degree in Nursing/Equivalent Additional Information Benefits ANNUAL GROSS SALARY
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English level C1/ C2 EXPERIENCE Experience in project management position, especially in the biomedical field. Experience in the biomedical sector, clinical trials or research projects. Specific
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and their quality control: -Participation in the medication management process. -Preparation and shipment of clinical trial patient samples -Support in the monitoring visits of the clinical trials