Clinical Research Coordinator II
2 days ago
Cedars-Sinai is seeking a highly skilled Clinical Research Coordinator II to join our team in Pediatric Neonatology. As a key member of our research team, you will be responsible for providing study coordination, screening patients for protocol eligibility, and participating in the informed consent process.
Key Responsibilities- Coordinate and manage clinical trials, including scheduling patients for research visits and procedures.
- Collaborate with physicians and medical personnel to document patient information on Case Report Forms (CRFs).
- Ensure accurate and timely data collection, documentation, entry, and reporting.
- Participate in monitoring and auditing activities, and notify direct supervisor of concerns regarding data quality and study conduct.
- Work closely with regulatory coordinators and the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters.
- Ensure compliance with federal and local agencies, including the Food and Drug Administration (FDA) and local Institutional Review Board.
- Maintain research practices using Good Clinical Practice (GCP) guidelines and patient confidentiality according to HIPAA regulations.
- High School Diploma/GED required; Bachelor's Degree in Science, Sociology, or related degree preferred; Master's Degree strongly preferred.
- SOCRA or ACRP certification preferred.
- Two (2) years of clinical research related experience required.
Cedars-Sinai is a leader in providing high-quality healthcare, encompassing primary care, specialized medicine, and research. We are committed to transforming healthcare for the benefit of patients and the community.
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Los Angeles, California, United States CEDARS-SINAI Full timeJob SummaryCedars-Sinai is seeking a highly skilled Clinical Research Coordinator II to join our team in Pediatric Neonatology. As a key member of our research team, you will be responsible for providing study coordination, screening potential patients for protocol eligibility, and participating in the informed consent process.Key Responsibilities:Coordinate...
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