Job Summary
A company is looking for a Clinical Data Coordinator for a remote, temporary position in Oncology research.
Key Responsibilities
- Manage the abstraction, entry, and oversight of study data for clinical trials
- Assist with the collection, cleaning, and reporting of clinical research data
- Ensure compliance with protocol guidelines and maintain study-specific documentation
Required Qualifications
- 3+ years of experience in data collection within a GCP/clinical research environment
- High School diploma required; some college preferred
- Experience in clinical studies, specifically in Oncology, for at least 6 months
- Familiarity with GCPs, ICH, and applicable federal regulations
- Experience with Medidata EDC systems and proficiency in Microsoft Office Suite
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