Top 139 Clinical research coordinator Jobs in Tarzana Ca

Lead Clinical Research Coordinator
Folio Clinical Research —Los Angeles, CA
- $75,000 - $90,000 a year
- 8 hour shift
- Background check
- 5 years
- Microsoft Office
- Health insurance
- Dental insurance
Quick Apply
3d
Referral Clinical Coordinator
OneLegacy —Mission Hills, 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 —El Segundo, CA
- $64,464.40 - $77,077.00 a year
- 12 hour shift
- LVN
- Hospital
- Mid-level
- Mileage reimbursement
- Health insurance
Quick Apply
Clinical Research Coordinator
Kelly Services —West Hills, CA
- $28 - $30 an hour
- Full-time
- CPR Certification
- BLS Certification
- HIPAA
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Assistant
Care Access —Santa Clarita, CA
- $19 - $33 an hour
- Spanish
- Vital signs
- Computer literacy
- Health savings account
- Paid holidays
Assistant Clinical Research Coordinator - Pediatrics
UCLA Health —Los Angeles, CA
- $29.28 - $47.10 an hour
- Word processing
- Computer literacy
- University
- Flexible schedule
Clinical Research Coordinator
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Mid-level
- Clinic
- Analysis skills
Clinical Research Coordinator – Pediatrics
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Mid-level
- Analysis skills
- Bachelor's degree
Assistant Clinical Research Coordinator - Hematology/Oncology (Santa Monica)
UCLA Health —Santa Monica, CA
- $30.74 - $49.46 an hour
- Clinic
- Analysis skills
- Bachelor's degree
16h
Clinical Research Coordinator - Pathology
UCLA Health —Los Angeles, CA
- Microsoft Excel
- Administrative experience
- Bachelor's degree
1d
Clinical Research Program Manager, Multi-Site Operations (Onsite)
Cedars-Sinai —Los Angeles, CA
- $45.56 - $77.45 an hour
- 8 hour shift
- High school diploma or GED
- Bachelor's degree
- Mentoring
Assistant Clinical Research Coordinator - Hematology/Oncology
UCLA Health —Los Angeles, CA
- $30.74 - $49.46 an hour
- Clinic
- Analysis skills
- University
Assistant Clinical Research Coordinator – Pediatrics
UCLA Health —Los Angeles, CA
- $30.74 - $49.46 an hour
- Weekends as needed
- Spanish
- Computer literacy
- English
Research Coordinator I
USC —Los Angeles, CA
- $32.01 - $36.06 an hour
- Psychiatry
- HIPAA
- Microsoft Office
Research Administrative Coordinator - Neurosciences
Cedars-Sinai —Los Angeles, CA
- $26.24 - $44.61 an hour
- 8 hour shift
- Mid-level
- Office
- High school diploma or GED
Clinical Research Coordinator - Hematology/Oncology (Santa Monica)
UCLA Health —Santa Monica, CA
- $38.19 - $61.45 an hour
- Mid-level
- Clinic
- Analysis skills
2d
Clinical Research Coordinator - Clinical Research
California Neuroscience Research, LLC —Sherman Oaks, CA
- $29 - $32 an hour
- Monday to Friday
- Blood sampling
- Vital signs
- Psychiatry
- Health insurance
- Dental insurance
Quick Apply
6d
Clinical Research Coordinator - Surgery
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Surgery
- Word processing
- Computer literacy
9d
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 Data Specialist I
USC —Los Angeles, CA
- $26.77 - $34.32 an hour
- Experience equivalent to degree accepted
- Associate's degree
- Medical terminology

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Lead Clinical Research Coordinator

Folio Clinical Research -
Los Angeles, CA

Quick Apply

Job Details

Full-time
$75,000 - $90,000 a year
3 days ago

Benefits

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

Qualifications

Optimizing workflow processes
Managing scientific research projects
Data integrity assurance
Clinical research methods
Clinical research
Presentation software
Research ethical considerations
Phlebotomy
Medical software
Safety regulations
Operations coordination
FDA 21 CFR Part 11
Phlebotomy specimen handling
Microsoft Office
Patient safety
Data quality management
Data integrity and documentation
ICH guidelines
Clinical research compliance
Bachelor's degree
Continuous improvement
Health information data integrity
Quality improvement
Data entry
Research compliance clinical trial records management
Clinical trials
Research regulatory compliance
Clinical quality assurance standards
Clinical research documentation
Achieving project delivery timelines

Full Job Description

Job description

Folio Clinical Research

Job: Lead Clinical Research Coordinator

Location: Los Angeles, CA (5x a week)

About Folio Clinical Research

Folio Clinical Research is a leading urologic research network treating urologic cancers, urinary stones, Peyronie’s disease, sexual and erectile dysfunction (ED), low testosterone, prostate disorders, urinary incontinence, and more. We partner with leading physician practices to create a cohesive, quality-oriented clinical culture, facilitating best practice sharing across our platform. Our affiliated practices gain access to a broad suite of clinical trials, providing significant benefits to both physicians and patients.

Position Overview

The Lead Clinical Research Coordinator (CRC) works directly under the supervision of the Principal Investigator (PI) to manage all aspects of clinical trial activities. The CRC is essential in facilitating and coordinating daily clinical trial activities, ensuring compliance, quality, and efficiency throughout the trial process. This role involves direct collaboration with the PI, sponsors, and other key stakeholders. The CRC will interact with patients during the recruitment and screening process. The CRC will also facilitate the informed consent process and provide ongoing participant support as needed.

About You:

Experienced Clinical Research Leader: You have a proven track record in managing clinical research operations, from feasibility assessments to study close-out.

Operational Expertise: You have deep experience managing day-to-day research site operations, ensuring adherence to protocol and regulatory standards

Mentorship Skills: You have training experience and can successfully collaborate with Principal Investigators, particularly those with minimal research experience.

Proactive Problem Solver: You always plan ahead and are proactive about having contingency strategies in place.

Business Acumen: You execute with a sense of urgency, maintaining a keen focus on both research objectives and business outcomes.

Commitment to Quality and Timeliness: You manage study timelines without compromising on quality.

Passion for Innovation: You are dedicated to bringing life-altering treatments to market, driven by patient outcomes.

Effective Communicator: You communicate clearly and regularly, keeping all stakeholders informed and ensuring a smooth study.

Self-Driven: You thrive with minimal supervision, taking ownership and responsibility for your deliverables.

Key Responsibilities:

Regulatory and Institutional Compliance: Support the Principal Investigator and relevant departments to ensure all clinical research activities comply with federal regulations, institutional policies, and sponsor requirements.

Documentation Management: Maintain secure and accurate storage of all study documents, including consent forms, case report forms, and investigational material records, in compliance with both sponsor and institutional requirements.

Study Oversight: Support the PI in ensuring the study meets compliance standards, including Institutional Review Board (IRB) approvals, health and safety requirements, conflict of interest disclosures, and adherence to financial terms.

Stakeholder Coordination: Maintain regular and effective communication with Sponsors, Contract Research Organizations (CROs), and internal team members (e.g., Investigators, Nurses, Medical Assistants) to facilitate study progress.

Meeting Participation: Engage in Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and other key study meetings as required.

Problem-Solving and Adaptation: Identify and anticipate potential obstacles to study timelines or deliverables, offering creative solutions to maintain momentum and study integrity.

Inventory and Equipment Management: Manage study-specific inventory, including identification, ordering, calibration, and secure storage of equipment required for the study.

Qualifications:

Minimum of five years of Clinical Research Coordinator experience.
Experience with various Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), and electronic Trial Master File (eTMF) systems.
Comprehensive understanding of urology and other associated therapeutic areas, medical terminology, to effectively execute clinical trials.
Deep knowledge of ICH-GCP, and regulatory requirements, with the ability to implement these effectively throughout the clinical trial.
Experience with data management processes, ensuring the accuracy and completeness of data collection, entry, and reporting, in line with Good Clinical Data Management Practices (GCDMP).
Experience ensuring and prioritizing patient safety and data integrity, embodying a commitment to the ethical conduct of clinical trials.
Experience maintaining the highest quality standards, while focusing on ongoing process improvements that lead to enhanced clinical trial efficiency and compliance.
Excellent interpersonal communication, both written and verbal. Can easily interface with team members and external stakeholders. Proven ability to develop positive relationships with internal teams, physicians, and external partners.
Strong attention to detail, and ability to handle multiple tasks simultaneously in a dynamic research environment.
Strong computer skills (MS Office, M PowerPoint, etc.) and software experience (CTMS, eTMF, EDC, IXRS, RTSM, etc.)
Ability to prioritize tasks, effectively manage time, and allocate resources efficiently to meet tight study deadlines.
Bachelor's degree or equivalent combination of education/experience in science or health-related field.

Any data provided as a part of this application will be stored in accordance with our Policy.

Folio Clinical Research is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

Job Type: Full-time

Benefits:

Health insurance
Dental insurance
Vision insurance
Paid time off

Medical Specialty:

Urology/oncology

Schedule:

8 hour shift
Monday to Friday

Education:

Bachelor's (Preferred)

Experience:

CRC: 5+ years (Required)

Work Location: In person

Job Type: Full-time

Pay: $75,000.00 - $90,000.00 per year

Benefits:

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

Application Question(s):

Will you now or in the future require sponsorship for employment visa status (e.g., H-1B, TN, etc.) to work in the United States?

Education:

Bachelor's (Preferred)

Experience:

Clinical Research Coordinating: 5 years (Preferred)
ICH-GCP: 5 years (Preferred)
EDC, CTMS, & eTMF: 5 years (Preferred)

Ability to Commute:

Los Angeles, CA 90048 (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

clinical research coordinator jobs in tarzana ca

Lead Clinical Research Coordinator

Referral Clinical Coordinator

Referral Clinical Coordinator

Clinical Research Coordinator

Clinical Research Assistant

Assistant Clinical Research Coordinator - Pediatrics

Clinical Research Coordinator

Clinical Research Coordinator – Pediatrics

Assistant Clinical Research Coordinator - Hematology/Oncology (Santa Monica)

Clinical Research Coordinator - Pathology

Clinical Research Program Manager, Multi-Site Operations (Onsite)

Assistant Clinical Research Coordinator - Hematology/Oncology

Assistant Clinical Research Coordinator – Pediatrics

Research Coordinator I

Research Administrative Coordinator - Neurosciences

Clinical Research Coordinator - Hematology/Oncology (Santa Monica)

Clinical Research Coordinator - Clinical Research

Clinical Research Coordinator - Surgery

Coordinator, Clinical Research Consortia

Clinical Research Data Specialist I

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