Posted 17 Jul 2025 (476 days ago) · Job 20471 · Read from the employer's Oracle career site, last checked 6 Nov 2026, 11:00 UTC

Clinical Research Coordinator I - Department of Neurology (Hybrid)

Cedars-Sinai · Los Angeles, California

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What the posting says

Each fact was read from this posting and checked:Statedin the posting, quotedConflictsposted two ways, both shownNot mentionedwe looked; it is not there

Employment typeStated
Full time
Work arrangementStated
Hybrid
ExperienceStated
0-2 years
EducationStated
['high school', 'bachelor degree', 'professional certificate']

Not mentioned in this posting

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PayNot mentioned
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ShiftNot mentioned
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Requirements, each with its sentence from the posting

These are the employer’s words. The index does not judge whether you meet them.

  • High School Diploma or GEDrequired

    High School Diploma/GED, requiredfrom the posting

  • Clinical research experiencerequired

    1 year of clinical research experience, requiredfrom the posting

  • Bachelor's degree in Science, Sociology, or related fieldpreferred

    Bachelor's degree in a Science, Sociology, or related field is preferredfrom the posting

  • ACRP/SOCRA certificationpreferred

    ACRP/SOCRA certification is preferredfrom the posting

  • Good Clinical Practice guidelinesimplied

    Maintains research practices using Good Clinical Practice (GCP) guidelinesfrom the posting

  • HIPAA complianceimplied

    Maintains strict patient confidentiality according to HIPAA regulations and applicable lawfrom the posting

  • Case Report Forms documentationimplied

    documents thoroughly on Case Report Forms (CRFs) information about changes in research participant conditionfrom the posting

Read the full posting as the employer wrote it

Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements!

Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world. Ranked among the best in the nation by U.S. News & World Report, our neurosurgeons and neurologists work together with experienced care teams to give patients the most effective treatment possible.

About the Role

This position will support the research programs in Department of Anesthesia and Neurology.

The Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The CRC I member is responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. This role is responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. The incumbent presents study information at research staff meeting. This position ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board.

Primary Duties and Responsibilities:

  • Scheduling of research participants for research visits and procedures.
  • In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) information about changes in research participant condition, adverse events, concomitant medication use, protocol compliance, and response to study drug.
  • Schedules and participates in monitoring and auditing activities.
  • 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 following local and federal guidelines.
  • May perform other regulatory/Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.
  • 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.
  • Coordinates training and education of other personnel.

Department-Specific Duties and Responsibilities:

  • Transportation of research medications.
  • Performs research study related assessments and questionnaires.
  • Assists with prescreening of research participants for various clinical trials.
  • Attends research meetings and monthly conference calls with sponsors for study updates.
  • Maintains organized paper and electronic research files.
  • Performs all data collection and data entry tasks for department clinical trials.
  • Assists with preparing manuscripts, letters, and other research documents as needed.
  • Responds to sponsor’ inquiries regarding protocol start-up activities and recruitment.
  • Performs literature reviews.

Qualifications

Education:

  • High School Diploma/GED, required.
  • Bachelor's degree in a Science, Sociology, or related field is preferred.

Licenses/Certifications:

  • ACRP/SOCRA certification is preferred.

Experience:

  • 1 year of clinical research experience, required.

About the organization

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. Today, Cedars- Sinai is known for its national leadership in transforming healthcare for the benefit of patients. 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.

The posting text is reproduced as the employer wrote it; the index adds nothing to it.