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data management sas edc quality control crf📋 Description
- Support the Lead DM to ensure timely tasks.
- May perform data entry for paper-CRF studies.
- May perform quality control of data entry.
- May develop CRF specifications from protocol and coordinate reviews.
- May assist in building clinical databases and UAT.
- Train staff on study CRFs, EDC, and related items.
🎯 Requirements
- Bachelor's degree or related experience.
- Around 2 years’ CDA experience in CRO/Pharma/Biotech.
- Proficiency in MS Word, Excel, PowerPoint, Outlook.
- Able to handle a variety of clinical research tasks.
- Excellent organizational and communication skills.
- Professional use of English; written and oral.
🎁 Benefits
- Global precision medicine company.
- Equal opportunity employer.
- Cross-functional training and collaboration.
- Travel may be required.
- Focus on data governance and quality.
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