Related skills
excel sas edc crf📋 Description
- Primary DM contact for assigned trials; ensure continuity and timely tasks.
- Oversee data entry with guidelines, training, and data quality controls.
- Lead UAT, CRF specs, and database development with stakeholders.
- Manage data quality, timelines, and resource planning.
- Train staff on CRF, EDC, and data management processes.
- Liaise with sponsors/vendors; travel may be required.
🎯 Requirements
- Bachelor's degree in a related field.
- 8+ years experience as Sr CDM or 5+ years as CDM II in CRO/Pharma/Biotech.
- Oncology experience preferred.
- Proficiency in MS Office: Word, Excel, PowerPoint, Outlook.
- Experience with clinical DBMS and knowledge of drug/device development.
- Strong leadership, communication, and organizational skills.
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