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studies. Job Responsibilities Coordinates clinical trials data management in compliance with federal regulations, GCP guidelines & internal policies. Ensures accurate & timely data compilation. Assists
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to compile an individual employment package every year. Discount with health insurers on supplemental packages. Flexible working week. Every year, 232 leave hours (at 38 hours). You can also sell or buy
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interpreting experiment results or research data, including assembly, compilation and summary of statistical and other data, as requested by the director supervisor(s) or PI. Processes blood sample, including
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