Top 189 Clinic coordinator Jobs in Mission Hills, 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
Intake Coordinator (Neuromodulation Division)
UCLA Health —Los Angeles, CA
- $35.47 - $48.82 an hour
- Full-time
- Microsoft Outlook
- Psychiatry
- Medical office experience
3d
Medical Eligibility and Intake Coordinator
Make-A-Wish Greater Los Angeles —Century City, CA
- $60,000 - $70,000 a year
- Email
- Hybrid work
- Background check
- Spanish
- Microsoft Excel
- 403(b) matching
- Paid holidays
Quick Apply
Intake coordinator
CNS —Agoura Hills, CA
- $25.24 - $35.00 an hour
- Part-time
- Microsoft Excel
- Microsoft Outlook
- Clinic
- Paid training
Quick Apply
Transplant Referral Coordinator
UCLA Health —Los Angeles, CA
- $30.36 - $43.49 an hour
- Microsoft Word
- Spanish
- Microsoft Excel
- Referral program
Medical Staff Coordinator - Medical Staff Admin
Providence —Mission Hills, CA
- $27.92 - $42.73 an hour
- 8 hour shift
- Mid-level
- Bachelor's degree
- Organizational skills
- Paid parental leave
- Paid holidays
3d
Neurosurgery Patient Care Coordinator
UCLA Health —Los Angeles, CA
- $26.42 - $37.49 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
Clinical Care Coordinator
Providence —Santa Monica, CA
- $25.00 - $37.98 an hour
- Full-time
- Mid-level
- Fair chance
- Paid parental leave
- Paid holidays
10d
Program Referrals Coordinator - Preventing and Ending Homelessness
Bet Tzedek Legal Services —Los Angeles, CA
- $82,718.17 - $86,496.61 a year
- Full-time
- Spanish
- Bachelor of Science
- English
- Profit sharing
- AD&D insurance
Quick Apply
Clinical Research Coordinator
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Mid-level
- Clinic
- Analysis skills
Care Coordinator
SCHARP —Los Angeles, CA
- $31.40 an hour
- Bilingual
- Mid-level
- Master's degree
Quick Apply
Care Coordinator - Davita IKC - Pasadena
DAVITA —Pasadena, CA
- $25.00 - $28.50 an hour
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Medical office experience
- Health insurance
- 401(k) matching
Support Coordinator II - Infusion Center - Full Time 8 Hour Days (Non-Exempt) (Non-Union)
Keck Medical Center of USC —Los Angeles, CA
- $26.00 - $41.28 an hour
- 8 hour shift
- Background check
- Spanish
- Microsoft Outlook
Care Coordinator - Davita IKC - Per Diem - L.A.
DAVITA —Los Angeles, CA
- $25.00 - $28.50 an hour
- 8 hour shift
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Medical office experience
- Health insurance
- 401(k) matching
Referrals - Referral Coordinator
Unicare Community Health Center —Los Angeles, CA
- $25 - $30 an hour
- Weekends as needed
- Spanish
- English
- Mid-level
Support Coordinator - Spine Center Cl - Full Time 8 Hour Days (Non-Exempt)(Union)
USC —Los Angeles, CA
- $21.00 - $35.36 an hour
- 8 hour shift
- Word processing
- Writing skills
- English
Concierge Patient Care Coordinator
Cenegenics —Beverly Hills, CA
- $29 - $32 an hour
- Full-time
- Merchandising
- Basic math
- HIPAA
- Paid jury duty
- Health savings account
Quick Apply
Support Coordinator II - Infusion Center - Full Time 8 Hour Days (Non-Exempt) (Non-Union)
USC —Los Angeles, CA
- $26.00 - $41.28 an hour
- 8 hour shift
- Spanish
- Microsoft Outlook
- Word processing
Administrative & Intake Coordinator
NATIONAL COUNCIL ON ALCOHOLISM —Santa Clarita, CA
- $23 - $25 an hour
- Full-time
- Spanish
- CPR Certification
- English
- Paid holidays
- Health insurance
Quick Apply
Support Coordinator II - Pavilion Multispec Cl - Full Time 8 Hour Days (Non-Exempt) (Non-Union)
Keck Medical Center of USC —Pasadena, CA
- $26.00 - $41.28 an hour
- 8 hour shift
- Background check
- Spanish
- Microsoft Outlook
11d

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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

clinic coordinator jobs in mission hills, ca

Clinical Research Coordinator I, Hybrid

Intake Coordinator (Neuromodulation Division)

Medical Eligibility and Intake Coordinator

Intake coordinator

Transplant Referral Coordinator

Medical Staff Coordinator - Medical Staff Admin

Neurosurgery Patient Care Coordinator

Clinical Care Coordinator

Program Referrals Coordinator - Preventing and Ending Homelessness

Clinical Research Coordinator

Care Coordinator

Care Coordinator - Davita IKC - Pasadena

Support Coordinator II - Infusion Center - Full Time 8 Hour Days (Non-Exempt) (Non-Union)

Care Coordinator - Davita IKC - Per Diem - L.A.

Referrals - Referral Coordinator

Support Coordinator - Spine Center Cl - Full Time 8 Hour Days (Non-Exempt)(Union)

Concierge Patient Care Coordinator

Support Coordinator II - Infusion Center - Full Time 8 Hour Days (Non-Exempt) (Non-Union)

Administrative & Intake Coordinator

Support Coordinator II - Pavilion Multispec Cl - Full Time 8 Hour Days (Non-Exempt) (Non-Union)

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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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