Top 206 Clinical research coordinator Jobs in Bell, Ca

Director of Clinical Research
The Practice Healthcare —Beverly Hills, CA
- $125,000 - $175,000 a year
- Full-time
- Surgery
- HIPAA
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator – Bilingual (Spanish-English) Foreign Grad MD welcome to apply
Confidential —Encino, CA
- $22 - $35 an hour
- Full-time
- Spanish
- Medicine
- HIPAA
- Paid holidays
- Health insurance
Quick Apply
Senior Clinical Research Coordinator
Ark Clinical Research —Fountain Valley, CA
- $35 - $40 an hour
- Full-time
- Spanish
- Nursing
- LVN
- Health insurance
- Dental insurance
Quick Apply
MA Clinical Coordinator
HRC Fertility Management, LLC —Pasadena, CA
- $28 - $30 an hour
- Full-time
- Writing skills
- Mid-level
- Organizational skills
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
Complete Care Community Health Center —Los Angeles, CA
- $40,000 - $60,000 a year
- Part-time
- HIPAA
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator I / COVID Recover
Children's Hospital Los Angeles —Los Angeles, CA
- $65,520 - $87,360 a year
- Full-time
- Spanish
- Databases
- High school diploma or GED
3d
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
Clinical Research Coordinator - Pediatrics
UCLA Health —Los Angeles, CA
- $36.37 - $58.52 an hour
- Mid-level
- Analysis skills
- University
Clinical Research Coordinator I
Children's Hospital Los Angeles —Los Angeles, CA
- $65,520 - $87,360 a year
- Full-time
- Spanish
- Databases
- High school diploma or GED
11d
Clinical Research Coordinator
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Word processing
- Computer literacy
- Mid-level
11d
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
Clinical Coordinator
Pacific Fertility Center Los Angeles —Glendale, CA
- $29 - $39 an hour
- Full-time
- Google Workspace
- Mid-level
- Clinic
- Free parking
- Health insurance
Quick Apply
Referral Clinical Coordinator
OneLegacy —El Segundo, CA
- $64,464.40 - $77,077.00 a year
- 12 hour shift
- LVN
- Hospital
- Mid-level
- Mileage reimbursement
- Health insurance
Quick Apply
Referral Clinical Coordinator
OneLegacy —Azusa, CA
- $58,604 - $70,707 a year
- 12 hour shift
- LVN
- Hospital
- Mid-level
- Mileage reimbursement
- Health insurance
Quick Apply
Clinical Research RN Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Exempt)
Keck Medical Center of USC —Arcadia, CA
- $49.86 - $76.69 an hour
- 8 hour shift
- Background check
- Nursing
- RN License
Research Lab Assistant - (Clinical Trials)
CenExel Clinical Research —Garden Grove, CA
- $20.00 - $21.50 an hour
- Full-time
- Psychiatry
- Writing skills
- High school diploma or GED
- Health savings account
- Health insurance
Quick Apply
Clinical Research Associate I, Dou Lab
Cedars-Sinai —Los Angeles, CA
- $25.00 - $33.51 an hour
- 8 hour shift
- HIPAA
- High school diploma or GED
- Bachelor's degree
Clinical Research Data Specialist I - Ouyang Lab
Cedars-Sinai —Los Angeles, CA
- $25.00 - $40.55 an hour
- 8 hour shift
- HIPAA
- Mid-level
- Analysis skills
Clinical Research Assistant, PRN
Care Access —Los Angeles, CA
- $34 - $44 an hour
- Part-time
- RN License
- Inventory management
- Pass drug screening
Heart Institute - Clinical Research Associate I, Susan Cheng Team
Cedars-Sinai —Los Angeles, CA
- $25.00 - $33.51 an hour
- 8 hour shift
- Ability to walk for extended periods
- Bachelor of Science
- Writing skills

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Director of Clinical Research

The Practice Healthcare -
Beverly Hills, CA

Quick Apply

Job Details

Full-time
$125,000 - $175,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching

Qualifications

Medical writing
Program design
Clinical study protocols and reports
Informed consent
Team leadership
Scientific research papers
Research project design
Team development
Research project technical leadership
Medical research
Bachelor's degree
Scientific protocols
Informed consent procedures implementation
Managing clinical research teams
Mentoring
Relationship management
Leading team collaboration initiatives
Clinical trial standard operating procedures
Communication with regulatory authorities for clinical trials
Clinical quality assurance standards
Training & development
Clinical research reports
Clinical consent forms
Ethical review application preparation
Journal article editing and review
Scientific reports

Full Job Description

About The Practice

The Practice Healthcare is a premier Beverly Hills surgical and aesthetic practice built around a team of nationally recognized, board-certified plastic and reconstructive surgeons. Our surgeons perform a high volume of breast reconstruction, aesthetic, and reconstructive procedures, and we hold one of the most valuable assets in clinical research: a large, longitudinal patient population and the outcomes that come with it.

We are now building a formal clinical research program from the ground up — and we’re hiring the person who will build it.

The Role

This is a rare opportunity to architect an entire research program from its foundations. As Director of Clinical Research, you will turn our surgeons’ case volume into a steady, credible stream of peer-reviewed publications and national conference presentations. You’ll stand up the infrastructure (SOPs, IRB relationships, regulatory binders, data systems), establish the workflows that capture patient outcomes, and recruit and manage the research fellows who help drive the output.

This is a hands-on builder role. In the early phase you will personally do the work — IRB submissions, study design support, data extraction oversight, manuscript shepherding — while putting the systems in place to scale a team behind you. You’ll partner directly with our surgeons, who serve as Principal Investigators, and you’ll be the operational and regulatory backbone that makes their research happen.

Our near-term mission is academic output and reputation: publications in journals like Plastic and Reconstructive Surgery and Aesthetic Surgery Journal, and podium and poster presentations at Plastic Surgery The Meeting (ASPS) and The Aesthetic Meeting. The role is focused on plastic, reconstructive, and aesthetic research; our wellness and longevity research is a future phase.

What You’ll Build

· A functioning research program where there is currently none — workflows, standards, and a publication pipeline.

· A regulatory foundation: standard operating procedures (SOPs), an Investigator Site File / regulatory binder, CITI/GCP training across the team, and an established relationship with a commercial IRB (e.g., Advarra or WCG).

· An outcomes-capture engine: enrollment in plastic surgery registries (e.g., ASPS/PSF TOPS, NBIR) and integration of validated patient-reported outcome measures (BREAST-Q, FACE-Q, BODY-Q) into our intake workflow.

· A research fellowship: a recruited, mentored, and managed cohort of research fellows producing abstracts and manuscripts.

· A publication and presentation pipeline that consistently moves projects from idea → IRB → data → abstract → podium/poster → published manuscript.

Key Responsibilities

Program development & operations - Build and own the research program’s infrastructure, SOPs, timelines, and quality standards. - Establish and manage the relationship with our commercial IRB; own all submissions, amendments, continuing reviews, and reporting. - Set up and maintain data-capture systems (e.g., REDCap) and the regulatory binder / essential documents. - Track and report on program performance (publications, abstracts, study cycle times, fellow productivity).

Regulatory & compliance - Serve as the practice’s regulatory point person: IRB compliance, HIPAA in research, informed consent and waivers, Good Clinical Practice (ICH-GCP), and Common Rule / FDA frameworks as applicable. - Maintain CITI/GCP training records, delegation-of-authority logs, and investigator documentation. - Safeguard data integrity, patient privacy, and ethical conduct across every study.

Research design & execution - Partner with surgeons (PIs) to scope and prioritize studies — retrospective chart reviews, outcomes registries, prospective studies, and patient-reported outcomes research. - Lead study design, protocol writing, data collection and management, and basic biostatistical analysis (or coordinate statistical support). - Drive projects to completion on realistic timelines.

Fellow & team leadership - Recruit, onboard, mentor, and manage research fellows; assign projects and hold them to publication and presentation targets. - Build the research function into a scalable team as the program grows.

Dissemination - Shepherd manuscripts and abstracts from draft to submission for target journals and national meetings. - Manage the submission calendar, authorship coordination, and conference logistics. - Build the practice’s academic reputation and research brand.

First-Year Priorities

1. Establish the IRB relationship, core SOPs, and regulatory infrastructure.

2. Get the team CITI/GCP-trained and the practice “research-ready.”

3. Launch the first wave of retrospective chart-review and registry projects using our existing patient data.

4. Integrate validated outcome measures (BREAST-Q et al.) into clinical workflow.

5. Recruit the initial research fellow(s) and deliver the program’s first abstracts/presentations.

Who You Are

Required - Demonstrated experience personally building or running a clinical research program or function, hands-on. - Hands-on command of the research lifecycle: IRB submissions, protocol development, informed consent, data management, and GCP/regulatory compliance. - Strong scientific writing and editing skills, with a track record of contributing to peer-reviewed publications and/or conference abstracts. - Comfort working independently and building from scratch — a self-starter who thrives without an existing playbook. - The interpersonal skill to partner with busy surgeons and the leadership to mentor and manage fellows. - Meticulous attention to detail, organization, and follow-through.

(We value proven experience over specific credentials. Bachelor’s degree required; advanced degree welcome but not mandatory.)

Preferred - Experience in surgical, plastic surgery, or aesthetic research specifically. - Familiarity with plastic surgery registries (TOPS, NBIR) and the Q-Portfolio outcome measures (BREAST-Q, FACE-Q, BODY-Q). - ACRP (ACRP-CP) or SOCRA (CCRP) certification — or willingness to obtain it (we’ll support certification). - Experience with REDCap or a comparable electronic data capture / CTMS system. - A network in the plastic and reconstructive surgery research community.

Why This Role

You’ll own this program from the start and shape every part of how it works. You’ll work alongside some of the most respected surgeons in the field, with an enviable volume of clinical material to study and a clear mandate to establish The Practice as a research leader. For the right person, this is a chance to build something lasting and put their name on it.

Pay: $125,000.00 - $175,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

clinical research coordinator jobs in bell, ca

Director of Clinical Research

Clinical Research Coordinator – Bilingual (Spanish-English) Foreign Grad MD welcome to apply

Senior Clinical Research Coordinator

MA Clinical Coordinator

Clinical Research Coordinator

Clinical Research Coordinator I / COVID Recover

Coordinator, Clinical Research Consortia

Clinical Research Coordinator - Pediatrics

Clinical Research Coordinator I

Clinical Research Coordinator

Clinical Research Assistant- Medical Oncology- Spanish Speaking

Clinical Coordinator

Referral Clinical Coordinator

Referral Clinical Coordinator

Clinical Research RN Coordinator - Clinical Research Institute - Full Time 8 Hours Day (Non-Union, Exempt)

Research Lab Assistant - (Clinical Trials)

Clinical Research Associate I, Dou Lab

Clinical Research Data Specialist I - Ouyang Lab

Clinical Research Assistant, PRN

Heart Institute - Clinical Research Associate I, Susan Cheng Team

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