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data management database sas edc quality control📋 Description
- Support data management across trials from start-up to post database lock.
- May perform data entry for paper-CRF studies and data QC.
- Develop CRF specifications and coordinate stakeholder feedback.
- Assist in building clinical databases and UAT with documentation.
- Specify requirements for edit checks (electronic/manual).
- Train staff on CRF/EDC; liaise with sponsors and vendors.
🎯 Requirements
- Bachelor's degree or related experience.
- Approximately 2 years of Clinical Data Associate experience.
- Proficiency with Microsoft Word, Excel, PowerPoint, Outlook.
- Strong organizational and communication skills.
- Professional English language skills (written and oral).
- Ability to manage multiple clinical research tasks.
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