Clinical Research Coordinator I
2 weeks ago
Cedars-Sinai is seeking a highly motivated and detail-oriented Clinical Research Coordinator I to join our Obstetrics & Gynecology Department. The successful candidate will be responsible for coordinating clinical research studies, ensuring compliance with regulatory requirements, and maintaining accurate records.
Key Responsibilities- Coordinate clinical research studies, including screening of potential patients, presenting non-medical trial concepts, and participating in informed consent processes.
- Schedule patients for research visits and procedures, and collaborate with physicians and medical personnel to document patient information.
- Maintain accurate source documents, data collection, documentation, entry, and reporting, including timely responses to sponsor queries.
- Compile and report on each study, including information related to protocol activity, accrual data, workload, and other research information.
- Ensure compliance with federal and local agencies, including the FDA and local IRB.
- Participate in required training and education programs, and maintain research practices using Good Clinical Practice (GCP) guidelines.
- Maintain patient confidentiality according to HIPAA regulations and applicable law.
Educational Requirements:
- High School Diploma/GED required
- Bachelor's Degree in Science, Sociology, or related field preferred
Licenses:
- SOCRA or ACRP Certification preferred upon hire
Experience:
- One (1) year of clinical research-related experience required
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