Clinical Research Associate I (CRA I) - Oncology Monitoring
Overview
The Clinical Research Associate I (CRA I) supports oncology solid tumor trial monitoring onsite. This full‑service CRO role ensures protocol compliance GCP ICH guidelines. The position protects patient safety and drives high‑quality data.
What You'll Do9
- 1Conduct site selection initiation routine and close‑out monitoring visits
- 2Verify protocol adherence and escalate quality concerns
- 3Review essential documents and oversee data entry queries
- 4Maintain Trial Master File and Investigator Site File
- 5Train and communicate with investigative sites
- 6Support recruitment planning and site‑level finances
- 7Prepare monitoring reports and follow‑up letters
- 8Collaborate with internal project teams for cohesive execution
- 9Contribute to site startup activities as needed
Requirements5
- 1Bachelor’s degree in science or healthcare preferred
- 26 months –2 years relevant experience or equivalent training
- 3Basic knowledge of GCP ICH regulations
- 4Ability to travel as required
- 5Minimum 5+ years of experience building ETL pipelines with Spark and Airflow
Salary Insight
$72 - $145k per year
Location
Required Skills
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