Clinical Research Associate I
Job Summary
To support clinical trials in the ENT department, the part-time Clinical Research Associate I will manage study protocols, ensure compliance with regulatory requirements, and assist in data collection and analysis remotely.
Key responsibilities
- Manage and oversee study protocols for clinical trials in the ENT department
- Ensure compliance with regulatory requirements and institutional policies
- Assist in data collection, analysis, and reporting for clinical research projects
Required qualifications
- Bachelor's degree in a relevant field such as life sciences or healthcare
- Experience in clinical research or a related area
- Knowledge of Good Clinical Practice (GCP) guidelines
- Familiarity with regulatory submissions and documentation
- Ability to work independently and manage multiple tasks effectively
Complete Job Description
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