Clinical Research Coordinator
Job Summary
To support clinical trials, the full-time Clinical Research Coordinator will manage study protocols, coordinate participant recruitment, and ensure compliance with regulatory requirements in an onsite role.
Key responsibilities
- Manage and oversee clinical trial protocols and study timelines
- Coordinate participant recruitment and maintain communication with study subjects
- Ensure compliance with regulatory standards and institutional policies
Required qualifications
- Bachelor's degree in a relevant field, such as life sciences or healthcare
- Experience in clinical research or related healthcare settings
- Knowledge of Good Clinical Practice (GCP) guidelines
- Certification in clinical research (e.g., CRC or CCRA) preferred
- Familiarity with regulatory submissions and documentation processes
Complete Job Description
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