Clinical Data Associate II

📋 Description

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• Back-up to Lead DM; ensure continuity and timely tasks.
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• Data entry for paper-CRF studies as needed.
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• Quality control of data entry.
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• Develop CRF specs from protocol; coordinate reviews.
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• Assist in building clinical databases and UAT.
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• Run patient and study status and metric reporting.
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🎯 Requirements

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• Bachelors and/or related experience.
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• ~2 years’ CDA experience in CRO/Pharma/Biotech.
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• MS Office proficiency: Word, Excel, PowerPoint, Outlook.
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• Ability to handle a variety of clinical research tasks.
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• Excellent organizational and communication skills.
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• Professional English; written and oral.
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