Clinical Research Coordinator I
2 weeks ago
Cedars-Sinai is seeking a highly skilled Clinical Research Coordinator I to join our team. The successful candidate will be responsible for providing study coordination, screening potential patients for protocol eligibility, and presenting non-medical trial concepts and details.
Key Responsibilities- Coordinate clinical research studies, including screening patients for eligibility and presenting trial concepts and details.
- Schedule patients for research visits and procedures.
- Document patient information and study data accurately and efficiently.
- Collaborate with physicians and medical personnel to ensure accurate and timely data collection and reporting.
- Ensure compliance with federal and local regulations, including FDA and IRB guidelines.
- Participate in monitoring and auditing activities to ensure data quality and study integrity.
- Compile and report study data, including protocol activity, accrual data, and workload information.
- Notify supervisors of concerns regarding data quality and study conduct.
- High School Diploma/GED
- 6 months clinical research related experience
Cedars-Sinai is a leader in providing high-quality healthcare, encompassing primary care, specialized medicine, and research. We are committed to delivering coordinated, compassionate healthcare to our patients and communities.
About the TeamWe are a growing network of clinicians and physicians dedicated to improving healthcare in Los Angeles and beyond. Join us in our mission to transform healthcare for the benefit of our patients.
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