Top 437 Clinical data coordinator Jobs in Santa Monica 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
Clinical Data Review Coordinator
UCLA Health —Santa Monica, CA
- $95,400 - $208,300 a year
- Nursing
- RN License
- Mid-level
Assistant Clinical Research Coordinator - Pediatrics
UCLA Health —Los Angeles, CA
- $30.74 - $49.46 an hour
- Hybrid work
- Word processing
- Computer literacy
- Neurology
8d
Clinical Research Coordinator
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Word processing
- Computer literacy
- Mid-level
6h
Clinical Research Coordinator III (Hybrid)
Cedars-Sinai —Beverly Hills, CA
- $34.24 - $58.21 an hour
- 8 hour shift
- Hybrid work
- HIPAA
- High school diploma or GED
- Bachelor's degree
Clinical Research Coordinator I, Hybrid
Cedars-Sinai —Beverly Hills, CA
- $24.00 - $39.76 an hour
- 8 hour shift
- Hybrid work
- HIPAA
- Clinic experience
- Office
- Opportunities for advancement
14d
Clinical Research Coordinator - Hematology/Oncology
UCLA Health —Santa Monica, CA
- $38.19 - $61.45 an hour
- Mid-level
- Clinic
- Analysis skills
5d
Assistant Clinical Research Coordinator - Urology
UCLA Health —Los Angeles, CA
- $30.74 - $49.46 an hour
- Word processing
- Computer literacy
- Data entry
5d
Clinical Research Coordinator - Radiological Sciences
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Word processing
- Computer literacy
- Mid-level
1d
Clinical Research Coordinator - Neurology
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Word processing
- Computer literacy
- Mid-level
5d
Clinical Research Associate I, Hybrid
Cedars-Sinai —Beverly Hills, CA
- $24.00 - $32.86 an hour
- 8 hour shift
- Hybrid work
- HIPAA
- High school diploma or GED
- Bachelor's degree
8d
Data Coordinator
START Center for Cancer Research —Los Angeles, CA
- $25 - $35 an hour
- Monday to Friday
- Mid-level
- Office
- High school diploma or GED
- Health savings account
- Paid holidays
Quick Apply
2d
Coordinator, Clinical Research Consortia
Children's Hospital Los Angeles —Los Angeles, CA
- $70,304 - $99,341 a year
- Part-time
- Mid-level
- Bachelor's degree
- Pediatrics
Medical Staff Coordinator - Med Staff - Full Time 8 Hour Days (Non-Exempt) (Non-Union)
USC —Los Angeles, CA
- $34.32 - $56.19 an hour
- 8 hour shift
- Acute care
- Mid-level
- Office
Utilization Review Coordinator
Guidelight Health —Los Angeles, CA
- $70,000 - $80,000 a year
- Remote
- Nursing
- Mid-level
- Microsoft Office
- Wellness program
- Health savings account
Quick Apply
Clinical Research Coordinator II – Head & Neck (Hybrid Role)
Cedars-Sinai —Beverly Hills, CA
- $28.30 - $48.11 an hour
- 8 hour shift
- Hybrid work
- HIPAA
- Mid-level
- High school diploma or GED
Medical Staff Coordinator - Med Staff - Full Time 8 Hour Days (Non-Exempt) (Non-Union)
Keck Medical Center of USC —Los Angeles, CA
- $34.32 - $56.19 an hour
- 8 hour shift
- Acute care
- Background check
- Hospital
Clinical Quality Coordinator
Greater Good Health —El Segundo, CA
- $55,000 - $65,000 a year
- Hybrid work
- Surgery
- Mid-level
- Office
- Free parking
- Paid parental leave
Quick Apply
1d
Senior Clinical Research Coordinator - Department of Medicine - Office of Research Administration
UCLA Health —Los Angeles, CA
- $93,927.51 - $151,099.73 a year
- Management
- Word processing
- Computer literacy
Assistant Clinical Research Coordinator – Pediatrics
UCLA Health —Los Angeles, CA
- $30.74 - $49.46 an hour
- Weekends as needed
- Spanish
- Computer literacy
- English
8d

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Experienced Clinical Research Coordinator

Proscience Research Group -
Culver City, CA

Quick Apply

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 data coordinator jobs in santa monica ca

Experienced Clinical Research Coordinator

Clinical Data Review Coordinator

Assistant Clinical Research Coordinator - Pediatrics

Clinical Research Coordinator

Clinical Research Coordinator III (Hybrid)

Clinical Research Coordinator I, Hybrid

Clinical Research Coordinator - Hematology/Oncology

Assistant Clinical Research Coordinator - Urology

Clinical Research Coordinator - Radiological Sciences

Clinical Research Coordinator - Neurology

Clinical Research Associate I, Hybrid

Data Coordinator

Coordinator, Clinical Research Consortia

Medical Staff Coordinator - Med Staff - Full Time 8 Hour Days (Non-Exempt) (Non-Union)

Utilization Review Coordinator

Clinical Research Coordinator II – Head & Neck (Hybrid Role)

Medical Staff Coordinator - Med Staff - Full Time 8 Hour Days (Non-Exempt) (Non-Union)

Clinical Quality Coordinator

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

Assistant Clinical Research Coordinator – Pediatrics

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