Related skills
data management sas edc clinical trials crf📋 Description
- Lead DM for assigned projects; ensure back-up and timely tasks
- Oversee data entry with guidelines, training, and quality
- Conduct database build and QA; ensure database quality
- Develop CRF specs from protocol and coordinate stakeholder feedback
- Manage timelines, resources, and meet DM deadlines
- Oversee edit checks and manual data review specs
🎯 Requirements
- Bachelor's degree or related experience
- 8+ years as Sr CDM or 5+ years as CDM II in CRO/Pharma/Biotech
- Oncology experience preferred
- Proficiency in MS Office: Word, Excel, PowerPoint, Outlook
- Excellent organizational and communication skills
- Experience with DM systems; SAS programming experience a plus
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