Clinical Research Coordinator I
2 weeks ago
Cedars-Sinai is seeking a highly motivated and detail-oriented Clinical Research Coordinator I to join our Alzheimer's and Dementia Research Program in the Department of Neurology. The successful candidate will work closely with an interdisciplinary team of neurologists, neuropsychologists, and clinical researchers to oversee studies related to the Memory Disorders Program.
The Clinical Research Coordinator I will be responsible for conducting phone screenings, coordinating visits, obtaining informed consent, conducting clinical research procedures, and assisting with regulatory responsibilities. The incumbent will also be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting. Additionally, the CRC will present study information at regular research staff meetings and ensure compliance with all federal and local agencies.
Key Responsibilities- Scheduling research visits and procedures for research participants.
- Collaborating with physicians and medical personnel to document changes in research participant condition, adverse events, concomitant medication use, protocol compliance, and response to study drug.
- Maintaining accurate source documents related to all research procedures.
- Scheduling and participating in monitoring and auditing activities.
- Notifying direct supervisor about concerns regarding data quality and study conduct.
- Working independently with external study monitors and/or auditors.
- Collaborating with regulatory coordinators or directly with the Institutional Review Board (IRB) to submit initial applications, amendments, continuing reviews, Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
- May involve other regulatory / IRB duties, budgeting duties, and assisting with research participant billing and reconciliation.
- May supervise Clinical Research Associates on data entry, data query, and resolution.
- Maintaining research practices using Good Clinical Practice (GCP) guidelines.
- Maintaining strict research participant confidentiality according to HIPAA regulations and applicable law.
- Participating in required training and education programs.
Education:
- High School Diploma/GED is required.
- Bachelor degree in Science, Sociology or related degree is strongly preferred.
Licenses/Certifications:
- ACRP/SoCRA (or equivalent) certification is preferred.
Experience:
- One year of clinical research or coordinating clinical research trials experience is required.
Cedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research. Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service.
Cedars-Sinai impacts the future of healthcare by developing new approaches to treatment and educating tomorrow's health professionals. Additionally, Cedars-Sinai demonstrates a commitment to the community through programs that improve the health of its most vulnerable residents.
About the TeamCedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest level of care to people in the Los Angeles that need our care the most.
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