Top 65 research coordinator Jobs in ucla ca

Clinical Research Coordinator II, Hybrid
Cedars-Sinai —Beverly Hills, CA
- $28.30 - $48.11 an hour
- 8 hour shift
- Hybrid work
- Patient monitoring
- HIPAA
- Mid-level
Research Coordinator - Neurology
UCLA Health —Los Angeles, CA
- $29.28 - $47.10 an hour
- Part-time
- Clinic
- Analysis skills
- Bachelor's degree
Senior Clinical Research Coordinator - Department of Medicine - Office of Research Administration
UCLA Health —Los Angeles, CA
- $89,454.77 - $143,904.50 a year
- Management
- Word processing
- Analysis skills
Assistant Clinical Research Coordinator - Urology
UCLA Health —Los Angeles, CA
- $29.28 - $47.10 an hour
- Mid-level
- Clinic
- Analysis skills
Clinical Research RN Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Exempt)
Keck Medical Center of USC —Arcadia, CA
- $49.86 - $76.69 an hour
- 8 hour shift
- Background check
- Nursing
- RN License
Clinical Research Coordinator II
Care Access —Thousand Oaks, CA
- $60,000 - $90,000 a year
- Microsoft Word
- Vital signs
- Writing skills
- Health savings account
- Paid holidays
Clinical Research Coordinator – Surgery
UCLA Health —Los Angeles, CA
- $36.37 - $58.52 an hour
- Surgery
- Word processing
- Computer literacy
Clinical Research Coordinator II
Children's Hospital Los Angeles —Los Angeles, CA
- $70,304 - $116,563 a year
- Full-time
- Mid-level
- Pediatrics
- 1 year
CIBMTR Data Coordinator (Registry Reporting)
UCLA Health —Los Angeles, CA
- $37.60 an hour
- Mid-level
- Bachelor's degree
- Medical terminology
Regulatory Coordinator - Urology
UCLA Health —Los Angeles, CA
- $31.51 - $62.64 an hour
- High school diploma or GED
- Analysis skills
- University
Regulatory Coordinator
Children's Hospital Los Angeles —Los Angeles, CA
- $51,979 - $85,394 a year
- Full-time
- Remote
- HIPAA
- Residential
- Bachelor's degree
Clinical Research Coordinator - Radiological Sciences
UCLA Health —Los Angeles, CA
- $36.37 - $58.52 an hour
- Mid-level
- 3 years
- Math
8d
Clinical Research Coordinator
Beverly Hills Oncology Me —Beverly Hills, CA
- $32 - $34 an hour
- Nursing
- Customer service
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Clinical Trials Regulatory Coordinator - Urology
UCLA Health —Los Angeles, CA
- $31.51 - $62.64 an hour
- Mid-level
- Analysis skills
- University
Clinical Research Coordinator I
Cedars-Sinai —Los Angeles, CA
- $27.18 - $42.13 an hour
- 8 hour shift
- HIPAA
- High school diploma or GED
- Bachelor's degree
Sr. Clinical Research Coordinator - Radiation Oncology
UCLA Health —Los Angeles, CA
- $6,892.14 - $11,089.02 a month
- Management
- Word processing
- Computer literacy
Experienced Clinical Research Coordinator
Greater Los Angeles Veterans Research and Education Foundation —Los Angeles, CA
- $21.06 - $31.40 an hour
- Part-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator (Oncology)
Flourish Research —Los Angeles, CA
- $31 - $43 an hour
- Weekends as needed
- Vital signs
- HIPAA
- Mid-level
- Paid holidays
- Disability insurance
7d
Research Coordinator (CHPLA)
Heluna Health —Los Angeles, CA
- $35.92 an hour
- Full-time
- Background check
- Spanish
- Addiction Medicine
Clinical Data Transfer Coordinator
COG Research Foundation, LLC —Arcadia, CA
- $64,542 - $92,421 a year
- Full-time
- Remote
- Microsoft Outlook
- Customer service
- Mid-level
- Paid holidays
- Health insurance
9d

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Clinical Research Coordinator II, Hybrid

Cedars-Sinai -
Beverly Hills, CA

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Job Details

$28.30 - $48.11 an hour

Qualifications

High school diploma or GED

Full Job Description

Job ID 16668 Location Beverly Hills, California, United States Job Category Academic / Research Date posted 05/04/2026

Job Description

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 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.
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. Primary Duties and Responsibilities
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

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 are

Minimum Requirements

High School Diploma/GED.
2 years Clinical research related experience.

Preferred Requirements

Bachelor's Degree

Req ID 16668

Working Title Clinical Research Coordinator II, 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 $28.30 - $48.11

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

research coordinator jobs in ucla ca

Clinical Research Coordinator II, Hybrid

Research Coordinator - Neurology

Senior Clinical Research Coordinator - Department of Medicine - Office of Research Administration

Assistant Clinical Research Coordinator - Urology

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

Clinical Research Coordinator II

Clinical Research Coordinator – Surgery

Clinical Research Coordinator II

CIBMTR Data Coordinator (Registry Reporting)

Regulatory Coordinator - Urology

Regulatory Coordinator

Clinical Research Coordinator - Radiological Sciences

Clinical Research Coordinator

Clinical Trials Regulatory Coordinator - Urology

Clinical Research Coordinator I

Sr. Clinical Research Coordinator - Radiation Oncology

Experienced Clinical Research Coordinator

Clinical Research Coordinator (Oncology)

Research Coordinator (CHPLA)

Clinical Data Transfer Coordinator

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Diversity and Inclusion at Cedars-Sinai

Cedars-Sinai is an Equal Employment Opportunity employer.

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