Job Summary
A company is looking for a Clinical Research Coordinator II to support oncology research studies.
Key Responsibilities
- Coordinate patient interactions, scheduling, consent, and visit management for research studies
- Maintain regulatory documentation and ensure compliance with study protocols and industry standards
- Assist in data management and preparation of reports for regulatory agencies
Required Qualifications
- Bachelor's Degree in a medical or science-related field
- 2 years of clinical research experience, with consideration for additional experience or advanced degrees
- Basic Life Support (BLS) certification may be required based on study protocols
- CPR AED certification may be required based on study protocols
- ACRP or SOCRA certification is preferred
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