Top 134 Clinical trial monitor Jobs in Los Angeles 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
4d
Clinical Trials Data Coord
City of Hope —Duarte, CA
- $30.67 - $47.54 an hour
- Full-time
- Remote
- HIPAA
- Mid-level
- Bachelor's degree
8d
Clinical Study Coordinator
City of Hope —Duarte, CA
- $44.90 - $69.60 an hour
- Full-time
- HIPAA
- Mid-level
- Bachelor's degree
Program Director, Forensic Community Treatment Center - Licensed Psychologist
GATEWAYS HOSPITAL & MENTAL HEALTH CENTER —Glendale, CA
- $140,000 - $150,000 a year
- Full-time
- Writing skills
- Outpatient experience
- Driver's License
- Health insurance
- Dental insurance
Quick Apply
Office Manager
California Institute of Aesthetic Arts —Los Angeles, CA
- $90,000 a year
- Full-time
- Background check
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
BCBA Social Skills Lead
Easter Seals Southern California, Inc. —Gardena, CA
- $78,000 a year
- Full-time
- LMFT
- Microsoft Excel
- Microsoft Outlook
Regulatory Coordinator II (Remote)
Cedars-Sinai —Beverly Hills, CA
- $34.24 - $58.21 an hour
- 8 hour shift
- Remote
- HIPAA
- Mid-level
- 3 years
Research Associate I - Guerin Children's - Traver Lab - Full-Time, On-Site
Cedars-Sinai —Los Angeles, CA
- $24.00 - $29.87 an hour
- 8 hour shift
- No experience needed
- Bachelor's degree
- Children
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
Quick Apply
Clinical Research Associate II - FSP
Precision for Medicine —Los Angeles, CA
- $91,500 - $137,300 a year
- Online Application
- Remote
- Clean driving record
- Word processing
- Mid-level
Quick Apply
Phlebotomist
ECN Operating LLC —Pasadena, CA
- $19 an hour
- Full-time
- Entry level
Quick Apply
Clinical Research Coordinator II
Helios Clinical Research —Cerritos, CA
- Full-time
- Vital signs
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Research Coordinator
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Mid-level
- Clinic
- Analysis skills
Clinical Study Coord
City of Hope —Duarte, CA
- $44.90 - $69.60 an hour
- Full-time
- HIPAA
- Mid-level
- Bachelor's degree
Research Associate I - Tourtellotte Lab - Pathology
Cedars-Sinai —Los Angeles, CA
- $24.00 - $29.87 an hour
- 8 hour shift
- No experience needed
- Bachelor's degree
- Cleaning
Clinical Research Associate II - FSP
Precision Medicine Group —Los Angeles, CA
- $91,500 - $137,300 a year
- Online Application
- Remote
- Clean driving record
- Word processing
- Mid-level
Clinical Study Coord-GU
City of Hope —Duarte, CA
- $44.90 - $69.60 an hour
- Full-time
- HIPAA
- Mid-level
- Bachelor's degree
CTMS Entry Coordinator
START Center for Cancer Research —Los Angeles, CA
- $24 - $26 an hour
- Monday to Friday
- Administrative experience
- High school diploma or GED
- Travel
- Health savings account
- Paid holidays
Quick Apply
4d
Research Associate I - Ajami Lab - Department of Neurology
Cedars-Sinai —Los Angeles, CA
- $24.00 - $29.87 an hour
- 8 hour shift
- Computer literacy
- Bachelor's degree
- Neurology
Research Associate I - Surgery Chair
Cedars-Sinai —Los Angeles, CA
- $24.00 - $29.87 an hour
- 8 hour shift
- Microsoft Word
- Surgery
- Bachelor of Science
10d

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Experienced Clinical Research Coordinator

Proscience Research Group -
Culver City, CA

Quick Apply

Job Details

Full-time
$25 - $34 an hour
4 days ago

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 trial monitor jobs in los angeles ca

Experienced Clinical Research Coordinator

Clinical Trials Data Coord

Clinical Study Coordinator

Program Director, Forensic Community Treatment Center - Licensed Psychologist

Office Manager

BCBA Social Skills Lead

Regulatory Coordinator II (Remote)

Research Associate I - Guerin Children's - Traver Lab - Full-Time, On-Site

Clinical Research Program Manager

Clinical Research Associate II - FSP

Phlebotomist

Clinical Research Coordinator II

Clinical Research Coordinator

Clinical Study Coord

Research Associate I - Tourtellotte Lab - Pathology

Clinical Research Associate II - FSP

Clinical Study Coord-GU

CTMS Entry Coordinator

Research Associate I - Ajami Lab - Department of Neurology

Research Associate I - Surgery Chair

I want to receive the latest job alert for clinical trial monitor in los angeles ca

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