Job Summary
A company is looking for a Clinical Research Coordinator II (Regulatory/Remote).
Key Responsibilities:
- Assist in developing research project plans and prepare regulatory submissions for the Institutional Review Board (IRB)
- Coordinate the development of research materials and maintain compliance with protocol guidelines and regulatory requirements
- Evaluate and interpret clinical data, preparing reports and presentations on study progress and outcomes
Required Qualifications:
- Bachelor's degree or equivalent combination of education and experience
- Basic Life Support certification required within one month of hire
- Minimum of 2 years of clinical research experience
- Experience with clinical study protocols and database management
- Knowledge of statistical analysis software (SAS) preferred
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