Job Summary
A company is looking for a Clinical Research Coordinator to support clinical trials and manage patient data.
Key Responsibilities
- Oversee the clinical trials start-up process, including protocol receipt and IRB submissions
- Manage data reporting, collection of source documents, and regulatory report preparation
- Coordinate clinical trials, ensuring compliance with protocol requirements and communication with sponsors
Required Qualifications
- Bachelor's Degree required, with 0-1 years of related experience preferred
- Experience in a medical or scientific research setting or a comparable technology-oriented environment preferred
- Ability to manage time effectively and prioritize workload
- Must adhere to confidentiality guidelines and practice discretion
- Proficiency in Microsoft Office and other computer skills required
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