Top 439 Clinical data Jobs in Woodland Hills, 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 Dietitian II
Children's Hospital Los Angeles —Los Angeles, CA
- $76,918.40 - $102,544.00 a year
- Full-time
- BLS Certification
- Mid-level
- Master's degree
BCBA Clinical Supervisor
Alongside ABA —Van Nuys, CA
- $85,000 - $95,000 a year
- Full-time
- School experience
- HIPAA
- Clinic experience
- Continuing education credits
- Paid holidays
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BCBA Clinical Supervisor
Alongside ABA —San Fernando, CA
- $85,000 - $95,000 a year
- Full-time
- School experience
- HIPAA
- Clinic experience
- Continuing education credits
- Paid holidays
Quick Apply
Clinical Coordinator (Dialysis RN)
Mission Hills Dialysis, LLC —Mission Hills, CA
- $85,000 - $115,000 a year
- Full-time
- Spanish
- CPR Certification
- Nursing
- Health insurance
- Dental insurance
Quick Apply
Clinical Dietitian II
Children's Hospital Los Angeles —Los Angeles, CA
- $76,918.40 - $102,544.00 a year
- Full-time
- BLS Certification
- Mid-level
- Master's degree
Clinical Manager (Dialysis RN)
Laurel Canyon Dialysis, LLC —Sun Valley, CA
- $85,000 - $115,000 a year
- Full-time
- Spanish
- CPR Certification
- Nursing
- Health insurance
- Dental insurance
Quick Apply
2d
BCBA/ Clinical Supervisor of Behavioral Services- Hybrid
Nurture & Nature ABA —Hawthorne, CA
- $90,000 - $110,000 a year
- Full-time
- Hybrid work
- Bilingual
- School experience
- Management
- Paid holidays
- Dental insurance
Quick Apply
Licensed Clinical Social Worker-Hybrid
Partners in Care Foundation, Inc. —Los Angeles, CA
- $36 - $42 an hour
- Full-time
- Hybrid work
- Background check
- Spanish
- Microsoft Outlook
- Health savings account
- Health insurance
Quick Apply
BCBA/ Clinical Supervisor of Behavioral Services- Hybrid
Nurture & Nature ABA —North Hollywood, CA
- $90,000 - $110,000 a year
- Full-time
- Hybrid work
- Bilingual
- School experience
- Management
- Paid holidays
- Dental insurance
Quick Apply
Pharmacy Clinical Systems Administrator
UCLA Health —Los Angeles, CA
- $39.93 - $69.93 an hour
- Monday to Friday
- System design
- Mid-level
- Bachelor's degree
Remote Clinical Social Worker (LMFT, LCSW, LPC, LPCC)
Telemynd —California
- From $70 an hour
- Choose your own hours
- Remote
- LMFT
- Licensed Clinical Social Worker
- Mid-level
- Flexible schedule
Quick Apply
ABA Associate Clinical Supervisor
Community Autism Services —San Fernando, CA
- $24 - $33 an hour
- Part-time
- Experience working with individuals with developmental disabilities
- Mid-level
- Children
- Paid training
- Referral program
Quick Apply
ABA Clinical Supervisor
BrightView Behavioral Health Services —Los Angeles, CA
- $32 - $38 an hour
- Part-time
- Spanish
- Writing skills
- Mid-level
- Paid holidays
- Paid time off
Quick Apply
PACE Clinical Consultant Pharmacist (Korean/English fluent) - Los Angeles, CA
Grane Rx —Los Angeles, CA
- Full-time
- Customer service
- Computer literacy
- Bachelor of Science
Clinical Psychologist (PsyD, PhD)
LifeStance Health —Marina del Rey, CA
- $136,000 - $182,000 a year
- Full-time
- Hybrid work
- Psychiatry
- Adults
- Clinic
- Paid parental leave
- Health insurance
Quick Apply
Licensed Clinical Social Worker (LCSW)
Benchmark Human Services —Los Angeles, CA
- $109,000 a year
- Online Application
- School experience
- Spanish
- CPR Certification
- Mileage reimbursement
- Health insurance
Quick Apply
Clinical Nursing Director
Commons Clinic —Marina del Rey, CA
- $155,000 - $175,000 a year
- Full-time
- Background check
- Nursing
- Surgery
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Assistant- Medical Oncology- ** Spanish Speaking**
Valkyrie Clinical Trials —Los Angeles, CA
- $39,000 - $50,000 a year
- 8 hour shift
- Spanish
- Maintenance
- Research
- Health insurance
- Dental insurance
Quick Apply
Child and Adolescent Clinical Psychologist (PsyD, PhD) (copy)
LifeStance Health —Burbank, CA
- $136,000 - $182,000 a year
- Full-time
- Hybrid work
- Psychiatry
- Adults
- Clinic
- Paid parental leave
- Health insurance
Quick Apply

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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 jobs in woodland hills, ca

Experienced Clinical Research Coordinator

Clinical Dietitian II

BCBA Clinical Supervisor

BCBA Clinical Supervisor

Clinical Coordinator (Dialysis RN)

Clinical Dietitian II

Clinical Manager (Dialysis RN)

BCBA/ Clinical Supervisor of Behavioral Services- Hybrid

Licensed Clinical Social Worker-Hybrid

BCBA/ Clinical Supervisor of Behavioral Services- Hybrid

Pharmacy Clinical Systems Administrator

Remote Clinical Social Worker (LMFT, LCSW, LPC, LPCC)

ABA Associate Clinical Supervisor

ABA Clinical Supervisor

PACE Clinical Consultant Pharmacist (Korean/English fluent) - Los Angeles, CA

Clinical Psychologist (PsyD, PhD)

Licensed Clinical Social Worker (LCSW)

Clinical Nursing Director

Clinical Research Assistant- Medical Oncology- Spanish Speaking

Child and Adolescent Clinical Psychologist (PsyD, PhD) (copy)

I want to receive the latest job alert for clinical data in woodland hills, ca

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