Related skills
data management sas edc clinical trials crf📋 Description
- Provide data management support from study start-up to database lock.
- May perform paper-CRF data entry and data QC.
- Develop CRF specs and coordinate stakeholder feedback.
- Build/maintain clinical databases; conduct UAT and related docs.
- Assist SAS programming and QC of SAS programs.
- Communicate with sponsors, vendors, and project teams; may travel.
🎯 Requirements
- Bachelor's degree or equivalent experience.
- 2-4 years clinical data management experience.
- Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
- Excellent organizational and communication skills; professional English.
- Able to handle a variety of clinical research tasks.
- Preferred: experience in clinical/healthcare discipline.
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