Top 793 Clinical care coordinator Jobs in Long Beach, Ca

Clinical Research Coordinator I, Hybrid
Cedars-Sinai —Beverly Hills, CA
- $25.00 - $40.55 an hour
- 8 hour shift
- Hybrid work
- HIPAA
- Clinic experience
- Office
- Opportunities for advancement
Heart Institute - Clinical Research Assoc I/CPT, Susan Cheng Team
Cedars-Sinai —Los Angeles, CA
- $25.00 - $33.51 an hour
- 8 hour shift
- Ability to walk for extended periods
- HIPAA
- Mid-level
Patient Care Coordinator Full-time
Lorian Health —Long Beach, CA
- $20 - $30 an hour
- Full-time
- Microsoft Excel
- Management
- Surgery
- Mileage reimbursement
- Fuel card
Quick Apply
Patient Care Coordinator
WEA CA PC —Los Angeles, CA
- $25 - $28 an hour
- Full-time
- Remote
- Spanish
- HIPAA
- English
Quick Apply
Clinical Program Coordinator, RN (Virtual Second Opinion) - Hybrid
Cedars-Sinai —Los Angeles, CA
- $116,000 - $170,000 a year
- 8 hour shift
- Hybrid work
- Nursing
- RN License
- Hospital
- Tuition reimbursement
1d
Home Care Coordinator
WelbeHealth —Carson, CA
- $70,304.00 - $89,535.30 a year
- Mid-level
- 3 years
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
9d
Scheduling Coordinator I
AltaMed Health Services Corporation —Long Beach, CA
- $25.75 - $32.19 an hour
- Full-time
- Background check
- Spanish
- English
- 403(b) matching
- Paid holidays
Nurse Navigator - DHI Administration - FT Days
University of California, Irvine —Orange, CA
- $68.86 - $100.34 an hour
- Full-time
- Background check
- Spanish
- Nursing
- Health insurance
- Retirement plan
Care Coordinator
SCHARP —Los Angeles, CA
- $31.40 an hour
- Bilingual
- Mid-level
- Master's degree
Quick Apply
Clinical Research Coordinator
Providence —Orange, CA
- $33.05 - $51.30 an hour
- Full-time
- Hospital
- Mid-level
- Trade school
- Paid parental leave
- Paid holidays
21h
Quality Assurance Coordinator - Hybrid
University of California, Irvine —Orange, CA
- $33.04 - $57.88 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
Registration Coordinator
Long Beach Memorial Medical Center —Long Beach, CA
- $22.89 - $33.18 an hour
- 8 hour shift
- Bilingual
- Hospital
- Mid-level
- Health insurance
Clinical Care Coordinator
Providence —Santa Monica, CA
- $25.00 - $37.98 an hour
- Full-time
- Mid-level
- Fair chance
- Paid parental leave
- Paid holidays
8d
Eligibility Specialist/Care Coordinator
Roots Through Recovery —Long Beach, CA
- $23 - $30 an hour
- Full-time
- Background check
- CPR Certification
- HIPAA
Quick Apply
Coordinator, Health Education
Children's Hospital Los Angeles —Los Angeles, CA
- $62,088 - $82,784 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Mid-level
- Bachelor's degree
18h
Clinical Research Coordinator - Hybrid
University of California, Irvine —Irvine, CA
- $37.56 - $61.91 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
TREATMENT PLAN COORDINATOR
Del Amo Behavioral Health System —Torrance, CA
- $45.34 - $68.02 an hour
- Full-time
- Nursing
- Adults
- Mid-level
- Health insurance
- Dental insurance
Support Coordinator II - Torrance Beach Cities Orthopedics Clinic - Full Time 8 Hour Days (Non-Exempt) (Non-Union)
USC —Torrance, CA
- $26.00 - $41.28 an hour
- 8 hour shift
- Spanish
- Microsoft Outlook
- Word processing
Client Services Coordinator - Outpatient Therapy
Long Beach Memorial Medical Center —Long Beach, CA
- $29 an hour
- 8 hour shift
- Spanish
- Microsoft Excel
- Microsoft Outlook
- Health insurance
10d
Care Manager - LVN
SCAN Health Plan —Lakewood, CA
- $34.47 - $55.14 an hour
- Full-time
- Remote
- Background check
- LVN
- Mid-level
- Wellness program
- Paid holidays
Quick Apply

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Clinical Research Coordinator I, Hybrid

Cedars-Sinai -
Beverly Hills, CA

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Job Details

$25.00 - $40.55 an hour

Benefits

Opportunities for advancement

Qualifications

High school diploma or GED
Oncology research
Oncology

Full Job Description

Job ID 18213 Location Beverly Hills, California, United States Job Category Academic / Research Date posted 07/08/2026

Job Description

Why Join Our Team
This is an excellent opportunity to work directly with patients while supporting innovative oncology clinical research. Clinical Research Coordinators collaborate closely with physicians and fellow research professionals, creating an environment where knowledge sharing, continuous learning, and teamwork are part of the day-to-day experience. The role also offers a defined career path, with opportunities for advancement from Clinical Research Coordinator I to Clinical Research Coordinator II and III.

Work Schedule & Environment
This is a hybrid position requiring a minimum of three onsite days per week. The standard schedule is 8-hour workdays, with overtime available or required based on business and study needs.

This role follows a hybrid work schedule; therefore, we can only consider applicants who are able to commute to our Los Angeles work location several times per week. If hired, you must reside within a commutable distance of the Los Angeles office.

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

Education

High School Diploma/GED - minimum
Bachelor's Degree Science, Sociology or related degree - preferred

Experience

1 year Clinical research related experience - minimum
Previous experience coordinating oncology research trials in a clinic and/or hospital setting.
Exceptional attention to detail with strong organizational and multitasking abilities.
Strong critical thinking and problem-solving skills.

Licenses and Certifications

No license or certification required - minimum
Certification In Clinical Research - Upon Hire preferred SOCRA or ACRP certification

Req ID 18213

Working Title Clinical Research Coordinator I, Hybrid

Department Cancer - SOCCI Clinical Research

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 $25 - $40.55

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 care coordinator jobs in long beach, ca

Clinical Research Coordinator I, Hybrid

Heart Institute - Clinical Research Assoc I/CPT, Susan Cheng Team

Patient Care Coordinator Full-time

Patient Care Coordinator

Clinical Program Coordinator, RN (Virtual Second Opinion) - Hybrid

Home Care Coordinator

Scheduling Coordinator I

Nurse Navigator - DHI Administration - FT Days

Care Coordinator

Clinical Research Coordinator

Quality Assurance Coordinator - Hybrid

Registration Coordinator

Clinical Care Coordinator

Eligibility Specialist/Care Coordinator

Coordinator, Health Education

Clinical Research Coordinator - Hybrid

TREATMENT PLAN COORDINATOR

Support Coordinator II - Torrance Beach Cities Orthopedics Clinic - Full Time 8 Hour Days (Non-Exempt) (Non-Union)

Client Services Coordinator - Outpatient Therapy

Care Manager - LVN

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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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