CEDARS-SINAI
Clinical Research Coordinator I – Community-Based Research (Korean Community)
CEDARS-SINAI, New York, New York, United States
Job Description
The Clinical Research Coordinator I will support the implementation of the community-based research study
ASPIRE (Asian American Prospective Research)
at the
Cancer Research Center for Health Equity (CRCHE)
and
Cedars-Sinai Community Outreach & Engagement . This position will play a key role in
developing community partnerships and coordinating the ASPIRE study as well as related community-based pilot studies . The CRC I will work specifically with
Korean communities within Cedars-Sinai’s catchment area , helping to foster trust, promote participation, and ensure culturally responsive engagement in cancer research and prevention initiatives. The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents study information at regular research staff meetings. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process. Schedules patients for research visits and procedures. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug. Maintains accurate source documents related to all research procedures. Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries. Schedules and participates in monitoring and auditing activities. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings. Notifies direct supervisor about concerns regarding data quality and study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines. May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law. Participates in required training and education programs
Qualifications
Requirements: High School Diploma/GED required. Bachelor's Degree preferred. 1 year Clinical research related experience required. Preferred Skills: Proven ability to develop and maintain relationships with key community organizations and stakeholders to support and promote community-based research initiatives. Experience representing programs at community events, conferences, health fairs, and other outreach activities to build partnerships, enhance visibility, and support participant recruitment efforts. Strong organizational skills to coordinate specific aspects of program planning and research implementation, ensuring adherence to timelines and achievement of defined outcomes. Ability to perform general office duties including photocopying, preparing informational packets, answering phones, and maintaining organized filing systems. Competence in assisting with data collection, conducting basic analysis, and contributing to the preparation of research reports and summaries. Strong written communication skills to draft professional emails, documents, and correspondence as needed. Physical ability to lift and carry items weighing up to 20 pounds. Flexibility to work occasional evenings and weekends based on program or research needs.
Req ID
: 12928 Working Title
: Clinical Research Coordinator I – Community-Based Research (Korean Community) Department
: Cancer - Research Center Health Equity Business Entity
: Cedars-Sinai Medical Center Job Category
: Academic / Research Job Specialty
: Research Studies/ Clin Trial Overtime Status
: NONEXEMPT Primary Shift
: Day Shift Duration
: 8 hour Base Pay
: $23.39 - $39.76
The Clinical Research Coordinator I will support the implementation of the community-based research study
ASPIRE (Asian American Prospective Research)
at the
Cancer Research Center for Health Equity (CRCHE)
and
Cedars-Sinai Community Outreach & Engagement . This position will play a key role in
developing community partnerships and coordinating the ASPIRE study as well as related community-based pilot studies . The CRC I will work specifically with
Korean communities within Cedars-Sinai’s catchment area , helping to foster trust, promote participation, and ensure culturally responsive engagement in cancer research and prevention initiatives. The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents study information at regular research staff meetings. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process. Schedules patients for research visits and procedures. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug. Maintains accurate source documents related to all research procedures. Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries. Schedules and participates in monitoring and auditing activities. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings. Notifies direct supervisor about concerns regarding data quality and study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines. May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law. Participates in required training and education programs
Qualifications
Requirements: High School Diploma/GED required. Bachelor's Degree preferred. 1 year Clinical research related experience required. Preferred Skills: Proven ability to develop and maintain relationships with key community organizations and stakeholders to support and promote community-based research initiatives. Experience representing programs at community events, conferences, health fairs, and other outreach activities to build partnerships, enhance visibility, and support participant recruitment efforts. Strong organizational skills to coordinate specific aspects of program planning and research implementation, ensuring adherence to timelines and achievement of defined outcomes. Ability to perform general office duties including photocopying, preparing informational packets, answering phones, and maintaining organized filing systems. Competence in assisting with data collection, conducting basic analysis, and contributing to the preparation of research reports and summaries. Strong written communication skills to draft professional emails, documents, and correspondence as needed. Physical ability to lift and carry items weighing up to 20 pounds. Flexibility to work occasional evenings and weekends based on program or research needs.
Req ID
: 12928 Working Title
: Clinical Research Coordinator I – Community-Based Research (Korean Community) Department
: Cancer - Research Center Health Equity Business Entity
: Cedars-Sinai Medical Center Job Category
: Academic / Research Job Specialty
: Research Studies/ Clin Trial Overtime Status
: NONEXEMPT Primary Shift
: Day Shift Duration
: 8 hour Base Pay
: $23.39 - $39.76