Top 559 Clinical data coordinator Jobs in Los Angeles Ca

Clinical Research Coordinator III (Hybrid)
Cedars-Sinai —Beverly Hills, CA
- $34.24 - $58.21 an hour
- 8 hour shift
- Hybrid work
- HIPAA
- High school diploma or GED
- Bachelor's degree
MDS Coordinator
Shoreline Healthcare Center —Long Beach, CA
- $45 - $55 an hour
- Weekends as needed
- Background check
- Skilled nursing facility
- LVN
- Health savings account
- Health insurance
Quick Apply
Medical Assistant - Clinical Research
CenExel Clinical Research —Torrance, CA
- $20.00 - $22.50 an hour
- Full-time
- Psychiatry
- Office
- Neurology
- Health savings account
- Health insurance
Quick Apply
4h
Patient Assistance Program Coordinator
OPN Healthcare —Glendale, CA
- $22 - $26 an hour
- Full-time
- Microsoft Word
- Background check
- Microsoft Excel
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator I, Laboratory (Onsite) + CPT1 - The Angeles Clinic & Research Institute
Cedars-Sinai —Los Angeles, CA
- $27.74 - $43.00 an hour
- 8 hour shift
- Hybrid work
- BLS Certification
- Mid-level
- High school diploma or GED
Clinical Data Review Coordinator
UCLA Health —Santa Monica, CA
- $95,400 - $208,300 a year
- Nursing
- RN License
- Mid-level
Clinical Research Coordinator I (Long Beach)
Irvine Clinical Research —Long Beach, CA
- $25 an hour
- Full-time
- Nursing
- Psychiatry
- English
- Dental insurance
- Paid time off
Quick Apply
Assistant Clinical Research Coordinator - Pediatrics
UCLA Health —Los Angeles, CA
- $29.28 - $47.10 an hour
- Word processing
- Computer literacy
- University
- Flexible schedule
Prior Authorization Coordinator
UCLA Health —Los Angeles, CA
- $30.36 - $43.49 an hour
- Computer literacy
- Data analysis skills
- High school diploma or GED
13d
Clinical Research Coordinator
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Mid-level
- Clinic
- Analysis skills
Clinical Research Coordinator I - Westside Los Angeles
Irvine Clinical Research —Los Angeles, CA
- $27 an hour
- Full-time
- Nursing
- English
- Master's degree
- Dental insurance
- Paid time off
Quick Apply
Research Assistant (Long Beach)
Irvine Clinical Research —Long Beach, CA
- $25 an hour
- Full-time
- English
- Clinic
- Neurology
- Dental insurance
- Paid time off
Quick Apply
Research Assistant - Westside Los Angeles
Irvine Clinical Research —Los Angeles, CA
- $25 an hour
- Full-time
- English
- Clinic
- Neurology
- Dental insurance
- Paid time off
Quick Apply
Clinical Research Associate I - Pulmonary Research Program/Lung Institute
Cedars-Sinai —Beverly Hills, CA
- $25.00 - $33.51 an hour
- 8 hour shift
- HIPAA
- High school diploma or GED
- Fair chance
8d
Clinical Research Coordinator I - Heart Institute - Bairey-Merz Lab
Cedars-Sinai —Los Angeles, CA
- $25.00 - $40.55 an hour
- 8 hour shift
- HIPAA
- High school diploma or GED
- Bachelor's degree
6d
Research Coordinator I
USC —Los Angeles, CA
- $32.01 - $36.06 an hour
- Psychiatry
- HIPAA
- Microsoft Office
Research Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Non-Exempt)
USC —Arcadia, CA
- $34.32 - $56.19 an hour
- 8 hour shift
- Word processing
- HIPAA
- Mid-level
Clinical Research Recruitment Coordinator
Irvine Clinical Research —Long Beach, CA
- $25 an hour
- Full-time
- Hybrid work
- Public speaking
- Clinic
- Older adults
- Dental insurance
- Paid time off
Quick Apply
Infection Control Coordinator - Quality Management - Full Time 8 Hour Day Shift (Non Union)
Keck Medical Center of USC —Glendale, CA
- $30 - $47 an hour
- 8 hour shift
- Background check
- Microsoft Excel
- Hospital
Coordinator, Clinical Research Consortia
Children's Hospital Los Angeles —Los Angeles, CA
- $70,304 - $99,341 a year
- Part-time
- Mid-level
- Bachelor's degree
- Pediatrics

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Clinical Research Coordinator III (Hybrid)

Cedars-Sinai -
Beverly Hills, CA

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Job Details

$34.24 - $58.21 an hour

Qualifications

High school diploma or GED

Full Job Description

Job ID 15479 Location Beverly Hills, California, United States Job Category Academic / Research Date posted 04/17/2026

Job Description

This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.

The Clinical Research Coordinator III 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 oversight of all studies with the group and the assignment of studies to clinical research personnel within the group, and supervision of research staff. Plans and coordinates strategies for increasing patient enrollment, improving efficiency, training of personnel, and 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 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.
Scheduling of 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 involve 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.
Works with Training and Education Coordinator to ensure all staff is properly trained and certified.
Participate in centralized activities such as auditing, Standard Operating Procedure development, etc.
Plans and coordinates strategies for increasing patient enrollment, and/or improving clinical research efficiency.
Identify quality and performance improvement opportunities and collaborate with staff in the development of action plans to improve quality.
Identifies new research opportunities and presents to investigators.
Supervises other research staff.

Qualifications

Minimum Requirements:

Education: High School Diploma/GED required.
4+ years of clinical research–related experience

Preferred Requirements:

Education: Bachelor’s Degree in Science, Sociology, or a related field preferred.

Req ID 15479

Working Title Clinical Research Coordinator III (Hybrid)

Department Cancer - SOCCI Clinical Research

Business Entity Cedars-Sinai Medical Center

Job Category Academic / Research

Job Specialty Research Studies/ Clin Trial

Overtime Status EXEMPT

Primary Shift Day

Shift Duration 8 hour

Base Pay $34.24 - $58.21

Diversity and Inclusion at Cedars-Sinai

We are caretakers and innovators committed to the pursuit of equitable healthcare. But health equity is not possible without representation. Our commitment to diversity goes beyond demographics or checking boxes. Our people must reflect the diverse identities, experiences and geographies of the communities and patients we serve – because that’s what our patients, colleagues and communities deserve Quality Care and Research—For All, By All.

Cedars-Sinai is an Equal Employment Opportunity employer.

Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at [email protected] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

Cedars-Sinai will consider for employment qualified applicants with criminal histories, in accordance with the Los Angeles Fair Chance Initiative for Hiring.

At Cedars-Sinai, we are dedicated to the safety, health and wellbeing of our patients and employees. This includes protecting our patients from communicable diseases, such as influenza (flu). For this reason, we require that all new employees receive a flu vaccine based on the seasonal availability of flu vaccine (typically during September through April each year) as a condition of employment, and annually thereafter as a condition of continued employment, subject to medical exemption or religious accommodation. For the same reason, you may also be required to receive other vaccines as a condition of employment. Cedars-Sinai reserves the right to make modifications to its required list of vaccines as required by law and/or policy.

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Refine Your Search

clinical data coordinator jobs in los angeles ca

Clinical Research Coordinator III (Hybrid)

MDS Coordinator

Medical Assistant - Clinical Research

Patient Assistance Program Coordinator

Clinical Research Coordinator I, Laboratory (Onsite) + CPT1 - The Angeles Clinic & Research Institute

Clinical Data Review Coordinator

Clinical Research Coordinator I (Long Beach)

Assistant Clinical Research Coordinator - Pediatrics

Prior Authorization Coordinator

Clinical Research Coordinator

Clinical Research Coordinator I - Westside Los Angeles

Research Assistant (Long Beach)

Research Assistant - Westside Los Angeles

Clinical Research Associate I - Pulmonary Research Program/Lung Institute

Clinical Research Coordinator I - Heart Institute - Bairey-Merz Lab

Research Coordinator I

Research Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Non-Exempt)

Clinical Research Recruitment Coordinator

Infection Control Coordinator - Quality Management - Full Time 8 Hour Day Shift (Non Union)

Coordinator, Clinical Research Consortia

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Job Description

Qualifications

Diversity and Inclusion at Cedars-Sinai

Cedars-Sinai is an Equal Employment Opportunity employer.

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