Related skills
sas edc quality control microsoft excel crf📋 Description
- Provide data management support from study start-up to post database lock.
- May perform data entry for paper-CRF studies and data QC.
- Develop CRF specifications and coordinate stakeholder feedback.
- Build/maintain databases; conduct database build UAT.
- Specify edit checks and maintain data management documentation.
- Train staff on CRF/EDC; liaise with sponsors/vendors; travel may be required.
🎯 Requirements
- Bachelor's degree or related experience.
- Around 2 years’ CDA experience in CRO/Pharma/Biotech.
- Proficiency in Microsoft Word, Excel, PowerPoint, Outlook.
- Able to handle diverse clinical research tasks.
- Excellent organizational and communication skills.
- Professional use of English (written and oral).
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