Related skills
sas edc sops crf📋 Description
- Lead data management for assigned trials; ensure backup and timely tasks.
- Oversee data entry process; guidelines, training, and QA.
- Develop CRF specifications from protocol; coordinate stakeholder feedback.
- Conduct UAT for database builds; ensure data quality and documentation.
- Train site personnel on CRF, EDC, and DM processes.
- Review data per Data Management Plan; monitor line listings and metrics.
🎯 Requirements
- Bachelors degree or related experience.
- 8+ yrs as Sr. CDM or 5+ yrs as CDM II (CRO/Pharma/Biotech).
- Oncology experience preferred.
- Proficient in MS Office (Word/Excel/PowerPoint/Outlook).
- Experience with clinical DBMS and data management.
- SAS programming experience beneficial; strong leadership.
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