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data management sas edc clinical trials sops📋 Description
- Lead DM for assigned trials; ensure continuity and timeliness
- Oversee data entry, guidelines, training, and resourcing
- Perform data entry QC and ensure data quality
- Develop CRF specifications from protocol; coordinate feedback
- Conduct DB build UAT and maintain DB documentation
- Manage timelines and resources to meet DM deadlines
🎯 Requirements
- Bachelor’s degree or related experience
- 8+ years as Sr. CDM or 5+ years as CDM II
- Oncology experience preferred
- Proficiency in MS Office (Word/Excel/PowerPoint/Outlook)
- Experience with clinical DBMS and SAS programming
- Ability to travel occasionally
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