Top 759 Development coordinator Jobs in Calabasas, 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
Service Coordinator - Bilingual; Armenian/English
Frank D. Lanterman Regional Center —Los Angeles, CA
- $5,413 - $7,950 a month
- Full-time
- Bilingual
- Experience working with individuals with developmental disabilities
- English
- Health insurance
- Dental insurance
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Patient Coordinator
GoodSkin Clinics —Los Angeles, CA
- From $95,000 a year
- Part-time
- Background check
- Hospitality
- Google Workspace
- Paid holidays
- Health insurance
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Deaf Blind Coordinator, Tactile ASL Interpreter
Braille Institute of America —Los Angeles, CA
- $26 - $30 an hour
- Part-time
- Classroom
- Experience working with individuals with disabilities
- Mid-level
- 403(b)
- Opportunities for advancement
Quick Apply
Product Development Coordinator
DTLA Private Label —Los Angeles, CA
- $24 - $29 an hour
- 8 hour shift
- Microsoft Excel
- Sales
- Customer service
- Health insurance
- Paid time off
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Apparel Product Development Coordinator
Harmony Brands Corp —Los Angeles, CA
- $28 - $31 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Ability to walk for extended periods
- Health insurance
- Dental insurance
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Activities Coordinator
NeuroRestorative —Los Angeles, CA
- $18.50 - $21.00 an hour
- Full-time
- Classroom
- Experience working with individuals with developmental disabilities
- High school diploma or GED
- Paid holidays
- Health insurance
14d
Resident Services Coordinator
LINC HOUSING CORPORATION —Inglewood, CA
- $22.33 - $26.27 an hour
- Weekends as needed
- Background check
- Spanish
- Addiction Medicine
- Disability insurance
- Health insurance
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Jewelry Production & Accounts Coordinator
Jewelry Group —Los Angeles, CA
- $20 - $25 an hour
- 8 hour shift
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Paid time off
- On-the-job training
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Program Coordinator
Dr. Yasmin Davidds Leadership Institute —Los Angeles, CA
- $55,000 a year
- Weekends as needed
- Hybrid work
- Mid-level
- Bachelor's degree
- Travel
- Paid holidays
- Paid time off
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11h
LMFT/LCSW Program Coordinator - Pathways to Recovery
Child & Family Center —Santa Clarita, CA
- $78,890 - $88,843 a year
- Full-time
- Hybrid work
- LMFT
- Spanish
- Addiction Medicine
- Wellness program
- AD&D insurance
Quick Apply
Coordinator, FSQA Customer Relations
Aspire Bakeries —Los Angeles, CA
- $19 - $23 an hour
- Bilingual
- Microsoft Excel
- Basic math
- Paid parental leave
- Health savings account
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6h
Office Coordinator/Medical Assistant
Valley Institute of Prosthetics and Orthotics —Newhall, CA
- $20 - $23 an hour
- Full-time
- Spanish
- Internal Medicine
- English
- Health insurance
- Dental insurance
Quick Apply
3d
Coordinator, Valuation
CIM Group, LP —Los Angeles, CA
- $26.44 - $31.25 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Wellness program
- Paid parental leave
Quick Apply
Sales Coordinator
Fruit Growers Supply —Valencia, CA
- $38,000 - $54,000 a year
- Full-time
- Microsoft Outlook
- High school
- Marketing
- Paid holidays
- Disability insurance
Quick Apply
Clinical Coordinator of Labor and Delivery
Clinical Management Consultants —North Hollywood, CA
- $120,020 - $140,020 a year
- Full-time
- Hospital
- Ob/Gyn
- Senior level
- Health insurance
- Tuition reimbursement
EXPERIENCED Dental Insurance & HYGEINE Coordinator
DR. HAD —Los Angeles, CA
- $24 - $32 an hour
- Part-time
- Spanish
- Dental office
- Customer service
- Dental insurance
Quick Apply
1d
Middle School Site Coordinator - Downtown L.A.
arc After School and Experiential Education —Los Angeles, CA
- $25 an hour
- 8 hour shift
- Background check
- Spanish
- CPR Certification
- AD&D insurance
- Paid holidays
Quick Apply
4h
Asbestos Abatement Coordinator
Project Support Services —Los Angeles, CA
- $90,000 - $105,000 a year
- Full-time
- School experience
- Construction site
- Engineering
- Paid holidays
- Health insurance
Quick Apply
6h
Accounting & Operations Coordinator
P1 Technologies —Manhattan Beach, CA
- $25 - $35 an hour
- Full-time
- Background check
- Mid-level
- Office
- Paid training
- Paid holidays
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

development coordinator jobs in calabasas, ca

Experienced Clinical Research Coordinator

Service Coordinator - Bilingual; Armenian/English

Patient Coordinator

Deaf Blind Coordinator, Tactile ASL Interpreter

Product Development Coordinator

Apparel Product Development Coordinator

Activities Coordinator

Resident Services Coordinator

Jewelry Production & Accounts Coordinator

Program Coordinator

LMFT/LCSW Program Coordinator - Pathways to Recovery

Coordinator, FSQA Customer Relations

Office Coordinator/Medical Assistant

Coordinator, Valuation

Sales Coordinator

Clinical Coordinator of Labor and Delivery

EXPERIENCED Dental Insurance & HYGEINE Coordinator

Middle School Site Coordinator - Downtown L.A.

Asbestos Abatement Coordinator

Accounting & Operations Coordinator

I want to receive the latest job alert for development coordinator in calabasas, ca

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