Clinical Research Coordintor II (Per Diem) - Chen Lab
Company: CEDARS-SINAI
Location: Los Angeles
Posted on: February 2, 2026
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Job Description:
Job Description Job Description The Smidt Heart Institute
reflects Cedars-Sinai's steadfast dedication to heart disease and
research innovation giving patients access to the highest level of
care. Year after year, thousands of people trust their hearts to
Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac
surgeons and specialized care teams treat the full spectrum of
heart disease and disorders, while our investigators continue to
advance the field with groundbreaking, life-saving research. From
genetic counseling and targeted drug therapies to a growing array
of minimally invasive procedures, Cedars-Sinai continues to stand
at the forefront of technology, innovation and discovery improving
patient outcomes. Are you ready to be a part of breakthrough
research? The Clinical Research Coordinator II works independently
providing study coordination including 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 information at regular research staff meetings. May plan
and coordinate strategies for increasing patient enrollment,
improving efficiency, training of personnel, or identifying new
research opportunities. Ensures compliance with all federal and
local agencies including the Food and Drug Administration (FDA) and
local Institutional Review Board (IRB). Primary Duties &
Responsibilities: - Independent study coordination including
assessing 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. - May coordinate training and
education of other personnel. - May participate in centralized
activities such as auditing, Standard Operating Procedure
development, etc. - May plan and coordinate strategies for
increasing patient enrollment, and/or improving clinical research
efficiency. - May identify quality and performance improvement
opportunities and collaborate with staff in the development of
action plans to improve quality. - May identify new research
opportunities and present to investigators. - Participates in
required training and education programs. Qualifications Education:
- High School Diploma is required. Bachelor's degree preferred in
Science, Sociology, or related field. Licenses and Certifications:
- Certification in Clinical Research from SOCRA or ACRP
certification is preferred. Experience: - 2 years of clinical
research related experience is required. Req ID : 14563 Working
Title : Clinical Research Coordintor II (Per Diem) - Chen Lab
Department : Heart Institute 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 : $28.30 - $48.11
Keywords: CEDARS-SINAI, Huntington Beach , Clinical Research Coordintor II (Per Diem) - Chen Lab, Healthcare , Los Angeles, California
