Top 1 Contract clinical research associate Jobs in West Hills Ca

Clinical Research Coordinator
System One —Inglewood, CA
- $26 - $30 an hour
- Contract
- CPR Certification
- Microsoft Excel
- BLS Certification
- Health insurance
- Dental insurance
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9d
Clinical Research Coordinator
System One —Inglewood, CA
Communicate with study participants to provide education, answer questions, and support adherence to study requirements.
$26 - $30 an hour
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Clinical Research Coordinator

System One -
Inglewood, CA

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Job Details

Contract
$26 - $30 an hour

Benefits

Health insurance
Dental insurance
401(k)
Vision insurance
Life insurance

Qualifications

High school diploma or GED

Full Job Description

Job Title: Clinical Research Coordinator
Location: Inglewood, California
Type: Contract
Compensation: $26.00-$30.00/hr
Work Model: 100% Onsite
Hours: 40.0

We are seeking a dedicated Clinical Research Coordinator to join our team in Inglewood, California. In this role, you will assist with the coordination and execution of clinical research studies, ensuring compliance with all regulatory guidelines. This position involves screening participants, managing study documentation, and supporting study procedures to ensure smooth operations. This is an onsite, contract opportunity offering engaging work in a dynamic research environment.

Responsibilities

Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff.
Conduct screening visits to collect medical history & other information from study participants.
Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines.
Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams.
Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards.
Communicate with study participants to provide education, answer questions, and support adherence to study requirements.
Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team.

Requirements

High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred.
Experience with participant screening and the informed consent process strongly preferred.
Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred.
Current CPR/BLS certification preferred.
Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

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Clinical Research Coordinator

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