Top 260 Clinical research assistant Jobs in Long Beach, Ca

Experienced Clinical Research Coordinator
Proscience Research Group —Culver City, CA
- $25 - $34 an hour
- Full-time
- Spanish
- Microsoft Excel
- Vital signs
- Health insurance
- 401(k)
Quick Apply
Quality Assurance Coordinator (Clinical Research)
CenExel Clinical Research —Los Alamitos, CA
- $30 - $33 an hour
- Full-time
- Background check
- Psychiatry
- Data analysis skills
- Health savings account
- Health insurance
Quick Apply
2h
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
1d
Clinical Research Site Operation Leader
Kelly Services —Inglewood, CA
- $95,000 - $130,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- 3 years
- Paid holidays
- Disability insurance
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Clinical Research Coordinator II - Pulmonary Research Program/Lung Institute
Cedars-Sinai —Los Angeles, CA
- $60,028.80 - $102,044.80 a year
- 8 hour shift
- HIPAA
- Mid-level
- High school diploma or GED
Research Assistant (Long Beach)
Irvine Clinical Research —Long Beach, CA
- $25 an hour
- Full-time
- English
- Clinic
- Neurology
- Dental insurance
- Paid time off
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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
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
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Clinical Research Coordinator I, Oncology
CHOC Children's —Orange, CA
- $29.48 - $48.61 an hour
- Full-time
- Microsoft Excel
- Writing skills
- Children
Clinical Research Associate
ICON Plc —Long Beach, CA
- $91,336 - $114,170 a year
- Full-time
- Remote
- Mid-level
- Bachelor's degree
- Travel
- Disability insurance
- Health insurance
Clinical Research Program Manager
LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA —Torrance, CA
- $85,000 - $130,000 a year
- HIPAA
- Mid-level
- Bachelor's degree
Research Assistant II
Helios Clinical Research —Cerritos, CA
- Full-time
- Vital signs
- Bachelor's degree
- No travel
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Clinical Research Coord II, Oncology
CHOC Children's —Orange, CA
- $30.94 - $51.05 an hour
- Full-time
- Microsoft Excel
- Hospital
- Writing skills
Clinical Research Coordinator
University of California, Irvine —Orange, CA
- $37.56 - $61.91 an hour
- Weekends as needed
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
Research Assistant - Hematology/Oncology
UCLA Health —Santa Monica, CA
- $30.74 - $49.46 an hour
- Clinic
- Analysis skills
- University
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
Research Lab Assistant - (Clinical Trials)
Collaborative Neuroscience Research, LLC —Garden Grove, CA
- $20.00 - $21.50 an hour
- Full-time
- Psychiatry
- Writing skills
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
Research Data Coordinator - Hybrid
University of California, Irvine —Orange, CA
- $37.56 - $61.91 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Retirement plan
IPH Clinical Research Coordinator
University of California, Irvine —Irvine, CA
- $37.56 - $42.55 an hour
- Full-time
- Background check
- HIPAA
- Mid-level
- Health insurance
- Retirement plan
2d
Research Admin Assistant - Clinical Research
Collaborative Neuroscience Research, LLC —Los Alamitos, CA
- $20.00 - $21.50 an hour
- Monday to Friday
- Psychiatry
- Office
- High school diploma or GED
- Disability insurance
- Health insurance
Quick Apply
13d

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Experienced Clinical Research Coordinator

Proscience Research Group -
Culver City, CA

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Job Details

Full-time
$25 - $34 an hour

Benefits

Health insurance
401(k)
Paid time off
Vision insurance
Flexible schedule
Retirement plan

Qualifications

Teamwork
HIPAA
English
Attention to detail
Organizational skills

Full Job Description

About Us ProScience Research Group is an established clinical research site located in Culver City, CA, specializing in psychiatric and central nervous system clinical trials. Our experienced investigators and research staff have extensive experience conducting clinical trials across Phase I through Phase IV in areas including depression, schizophrenia, schizoaffective disorder, bipolar disorder, ADHD, anxiety, insomnia, migraine, Alzheimer’s disease, and other CNS-related conditions. Our mission is to provide the highest quality research data while following all applicable regulations, Good Clinical Practice, and human subject protection standards, with patient safety as our highest priority. We are committed to advancing medicine by contributing to the development of new and improved therapies that may improve the quality of life for patients and their families.

Position Overview We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to join our clinical research team. This position offers the opportunity to work closely with experienced Board-Certified Psychiatrists, research physicians, registered nurses, clinical research coordinators, and highly experienced inpatient staff in the conduct of psychiatric and CNS clinical trials. Studies may include both outpatient and inpatient clinical trials, offering the CRC hands-on experience in a structured research environment while supporting participant safety, protocol compliance, regulatory readiness, and high-quality data collection.T he ideal candidate will have at least one year of prior clinical research experience, preferably in psychiatric, CNS, inpatient, or outpatient clinical trials. A strong regulatory skillset is highly preferred, including experience maintaining investigator site files, supporting IRB submissions, tracking essential documents, preparing for monitoring visits, and ensuring ongoing inspection readiness. We also welcome applicants with related healthcare or regulatory experience and a strong desire to learn.

Responsibilities

Collect and accurately document source data in accordance with protocol requirements
Coordinate study visits and ensure protocol-required procedures are completed accurately and on time
Manage EDC, IWRS/IVRS, RTSM, ePRO, eCOA, and other sponsor/CRO study platforms
Perform study-related procedures, including vital signs, ECGs, lab processing, and phlebotomy, if certified
Recruit, pre-screen, screen, and schedule study participants
Support participant retention and maintain strong communication with study participants
Assist with informed consent processes under investigator oversight
Support outpatient and inpatient study visits while working alongside experienced clinical and inpatient staff
Support study start-up activities, site initiation visits, interim monitoring visits, audits, and close-out visits
Maintain regulatory documents and investigator site files, including ISF/eISF documentation
Support IRB submissions, continuing reviews, amendments, safety reports, and other regulatory correspondence
Track and maintain essential documents, training records, delegation logs, CVs, licenses, and certifications
Ensure study documentation remains accurate, current, complete, and inspection-ready
Communicate regularly with sponsors, CROs, IRBs, vendors, monitors, and internal team members
Assist with investigational product accountability and study supply management, as applicable
Uphold HIPAA, GCP, human subject protection, and site SOP requirements
Maintain a professional and compassionate approach when working with psychiatric and CNS study populations

Preferred Qualifications

Minimum of 3 year of clinical research experience, preferably in pharmaceutical clinical trials
Strong regulatory experience strongly preferred
Experience maintaining ISF binders and essential regulatory documents
Knowledge of IRB submissions, amendments, continuing reviews, safety reports, and close-out documentation
Experience preparing for monitoring visits, audits, and sponsor/CRO quality reviews
Experience in psychiatry, CNS, behavioral health, inpatient, or outpatient research preferred
Familiarity with EDC, IWRS/IVRS, RTSM, ePRO, eCOA, and sponsor portals
Strong organizational skills, follow-through, and attention to detail
Excellent communication skills and professional bedside manner
Ability to work with diverse patient populations, including individuals with mental health conditions
Bilingual English/Spanish preferred
Proficiency with Microsoft Word, Excel, Outlook, and PowerPoint
GCP certification preferred
IATA certification preferred
Phlebotomy certification preferred but not required

Compensation & Benefits

Competitive salary based on experience
Health and Vision insurance
Paid time off
Flexible scheduling, as applicable
Professional development and clinical research growth opportunities
Supportive, team-oriented work environment

Why Join ProScience Research Group?At ProScience Research Group, you will be part of an experienced research team dedicated to conducting high-quality psychiatric and CNS clinical trials, including both outpatient and inpatient studies. You will have the opportunity to work alongside highly experienced investigators, coordinators, nurses, and inpatient staff who bring decades of psychiatric and clinical research experience to the site.This role is ideal for someone who is passionate about clinical research, enjoys working directly with patients, has strong regulatory skills, and wants to contribute to the advancement of new treatment options in mental health and CNS care.

Schedule & Location

Job Type: Full-time
Schedule: Monday to Friday, day shift
Work Location: In person
Location: Culver City, CA 90230

If you are passionate about clinical research, patient care, regulatory excellence, and advancing new treatment options in psychiatry and CNS medicine, we would love to hear from you.

Pay: $25.00 - $34.00 per hour

Benefits:

401(k)
Flexible schedule
Health insurance
Paid time off
Retirement plan

Work Location: In person

Quick Apply

Refine Your Search

clinical research assistant jobs in long beach, ca

Experienced Clinical Research Coordinator

Quality Assurance Coordinator (Clinical Research)

Medical Assistant - Clinical Research

Clinical Research Site Operation Leader

Clinical Research Coordinator II - Pulmonary Research Program/Lung Institute

Research Assistant (Long Beach)

Clinical Research Recruitment Coordinator

Clinical Research Coordinator I (Long Beach)

Clinical Research Coordinator I, Oncology

Clinical Research Associate

Clinical Research Program Manager

Research Assistant II

Clinical Research Coord II, Oncology

Clinical Research Coordinator

Research Assistant - Hematology/Oncology

Clinical Research Coordinator - Hybrid

Research Lab Assistant - (Clinical Trials)

Research Data Coordinator - Hybrid

IPH Clinical Research Coordinator

Research Admin Assistant - Clinical Research

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