Top 136 Clinical coordinator Jobs in San Francisco Bay Area Ca

Clinical Research Coordinator
Confidential —San Carlos, CA
- $30 - $45 an hour
- Part-time
- HIPAA
- Mid-level
- In-person
- Flexible schedule
Quick Apply
1d
Clinical Research Coordinator
University of California San Francisco —San Francisco, CA
- Full-time
- Mid-level
- High school diploma or GED
- University
Assistant Clinical Research Coordinator
University of California San Francisco —Oakland, CA
- Full-time
- Windows
- High school diploma or GED
- Children
Clinical Research Coordinator HEMONC
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Outlook
- HIPAA
- Mid-level
Clinical Research Coordinator
Nudge —San Francisco, CA
- Full-time
- Mid-level
- Bachelor's degree
- Experience equivalent to degree accepted
Clinical Research Coordinator (Osher Center)
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Excel
- Management
- Bachelor of Science
Clinical Research Coordinator (San Francisco)
University of California, Riverside —San Francisco, CA
- $34.37 - $55.27 an hour
- Full-time
- Microsoft Access
- Psychiatry
- Mid-level
- Free parking
- Disability insurance
Quick Apply
11d
Clinical Research Coordinator Cardiology
University of California San Francisco —San Francisco, CA
- HIPAA
- Mid-level
- High school diploma or GED
Radiography Clinical Coordinator
Aya Healthcare —San Francisco, CA
- $65 - $70 an hour
- 8 hour shift
- Background check
- Mid-level
- Supervising experience
- Health insurance
- Dental insurance
Quick Apply
1d
Clinical Coordinator (RN)
Satellite Healthcare, Inc —Oakland, CA
- $104,772.83 - $130,668.00 a year
- Full-time
- Nursing
- Microsoft Excel
- Microsoft Outlook
10d
Registered Nurse - Clinical Case Consultant - ECM
Pacific Health Group —California
- $85,000 - $95,000 a year
- Weekends as needed
- Hybrid work
- Background check
- Spanish
- Nursing
- AD&D insurance
- Paid holidays
Quick Apply
Senior Clinical Research Associate
Medasource —San Francisco, CA
- $70 - $80 an hour
- Full-time
- Travel
- Conflict management
- Organizational skills
Quick Apply
8d
Clinical Research Coordinator Nephrology
University of California San Francisco —San Francisco, CA
- Full-time
- HIPAA
- Mid-level
- High school diploma or GED
Clinical Research Coordinator Surgery
University of California San Francisco —San Francisco, CA
- Surgery
- Bachelor of Science
- Writing skills
Clinical Research Coordinator Associate
Stanford University —Redwood City, CA
- $34.56 - $40.30 an hour
- Weekends as needed
- Hybrid work
- Spanish
- HIPAA
- Mid-level
Clinical Research Coordinator (1/2)
University of California San Francisco —San Francisco, CA
- Full-time
- Mid-level
- Windows
- High school diploma or GED
3d
Assistant Clinical Research Coordinator
Stanford University —Redwood City, CA
- Extended hours
- Hybrid work
- Vital signs
- Office
- Administrative experience
5d
Associate Clinical Education Coordinator
Guardant Health —Redwood City, CA
- $57,205 - $92,550 a year
- Email
- Hybrid work
- Background check
- Mid-level
- Office
Clinical Research Coordinator (9611C), School of Optometry & Vision Science #87775
University of California Berkeley —Berkeley, CA
- $45.84 - $52.64 an hour
- Full-time
- Microsoft Word
- Clinic experience
- Mid-level
7d
Clinical Procurement Coordinator (RRT's, PA's & RN's Preferred)
Donor Network West —San Francisco, CA
- $65.74 - $74.13 an hour
- Full-time
- Hybrid work
- Nursing
- Mid-level
- ACLS Certification
- On-the-job training
Quick Apply

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Clinical Research Coordinator

Confidential
San Carlos, CA

Quick Apply

Job Details

Part-time | Full-time
$30 - $45 an hour
1 day ago

Benefits

Flexible schedule

Qualifications

HIPAA compliance
HIPAA
Schedule management
ICH guidelines
Attention to detail
Clinical quality assurance standards
Root cause analysis
Clinical confidentiality policies
Clinical trial support in drug product development
Pharmaceutical research experience
FDA regulations
Time management

Full Job Description

Clinical Research Coordinator (CRC)

Company: LClinical Research

Location: San Carlos, California

Position: Full-Time / Part-Time

About LClinical Research

LClinical Research is a growing clinical research organization dedicated to conducting high-quality clinical trials while maintaining patient safety, regulatory compliance, data integrity, and adherence to study protocols and Good Clinical Practice (GCP).

We are seeking an experienced, organized, and highly motivated Clinical Research Coordinator (CRC) to join our San Carlos research site and work closely with our Principal Investigator, research team, sponsors, CROs, and study participants.

Minimum Requirement

A minimum of 2 years of hands-on clinical trial experience as a Clinical Research Coordinator or in a comparable clinical research role is required.

Candidates without at least 2 years of clinical trial experience will not be considered for this position.

Key Responsibilities

Coordinate clinical trials from site initiation through study closeout.

Recruit, pre-screen, screen, and coordinate study participants.

Schedule and manage participant visits according to study protocols.

Review inclusion/exclusion criteria and assist the PI/Sub-Investigators with participant eligibility.

Facilitate and document the informed-consent process according to applicable regulations, IRB requirements, protocol, training, delegation, and site procedures.

Perform study procedures within appropriate training, delegation, and scope.

Collect and accurately document medical histories, medications, adverse events, and study-related information.

Complete and maintain source documentation, CRFs/eCRFs, and Electronic Data Capture (EDC) systems.

Respond to data queries accurately and within required timelines.

Maintain regulatory binders and essential study documents.

Assist with IRB submissions, amendments, continuing reviews, safety reports, and regulatory correspondence.

Coordinate laboratory specimen collection, processing, storage, packaging, and shipment.

Maintain investigational product/device accountability documentation when applicable and appropriately delegated.

Track study supplies, laboratory kits, equipment, and study materials.

Communicate professionally with sponsors, CROs, CRAs/monitors, central laboratories, pharmacies, and study vendors.

Prepare for and participate in Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), monitoring visits, audits, and closeout visits.

Maintain screening, enrollment, delegation, training, temperature, and other required study logs.

Assist with protocol deviations, root-cause analysis, and Corrective and Preventive Action (CAPA) documentation and implementation.

Ensure adverse events and serious adverse events are appropriately escalated and documented according to protocol requirements.

Maintain compliance with ICH-GCP, FDA regulations, HIPAA, IRB requirements, study protocols, and LClinical Research SOPs.

Work closely with the Principal Investigator to support appropriate study oversight and timely completion of study requirements.

Maintain strict participant confidentiality and professional standards.

Required Qualifications

Minimum 2 years of hands-on clinical trial/clinical research experience required.

Previous experience working as a Clinical Research Coordinator strongly preferred.

Experience with pharmaceutical-sponsored clinical trials preferred.

Knowledge of ICH-GCP, FDA regulations, HIPAA, and IRB requirements.

Experience with EDC and electronic clinical research platforms.

Strong understanding of source and regulatory documentation.

Excellent organizational and time-management skills.

Exceptional attention to detail and accuracy.

Ability to manage multiple studies, deadlines, and participant visits simultaneously.

Strong written and verbal communication skills.

Ability to communicate effectively with investigators, sponsors, CROs, monitors, and study participants.

Ability to work independently and collaboratively within a research team.

GCP and Human Subjects Protection training preferred.

Preferred Experience

Experience in one or more of the following is highly desirable:

Phase II–IV clinical trials

Endocrinology and metabolic disorders

Obesity and weight-management clinical trials

Diabetes

Osteoporosis and metabolic bone disorders

Patient recruitment and retention

Regulatory documentation

Sponsor/CRO monitoring visits

CAPA and audit readiness

Ideal Candidate

We are looking for someone who is reliable, proactive, highly organized, detail-oriented, and capable of taking ownership of assigned clinical trials.

The successful CRC will understand that excellent clinical research requires both outstanding participant care and meticulous documentation. The candidate must be comfortable working directly with the Principal Investigator and research team while ensuring that study activities are completed accurately, efficiently, and according to protocol.

How to Apply

Please submit your resume/CV through Indeed and include your years of clinical trial experience, types/phases of studies coordinated, EDC systems used, and relevant certifications.

Please apply only if you have a minimum of 2 years of clinical trial experience.

LClinical Research is an Equal Opportunity Employer.

Pay: $30.00 - $45.00 per hour

Benefits:

Flexible schedule

Work Location: In person

Quick Apply

Refine Your Search

clinical coordinator jobs in san francisco bay area ca

Clinical Research Coordinator

Clinical Research Coordinator

Assistant Clinical Research Coordinator

Clinical Research Coordinator HEMONC

Clinical Research Coordinator

Clinical Research Coordinator (Osher Center)

Clinical Research Coordinator (San Francisco)

Clinical Research Coordinator Cardiology

Radiography Clinical Coordinator

Clinical Coordinator (RN)

Registered Nurse - Clinical Case Consultant - ECM

Senior Clinical Research Associate

Clinical Research Coordinator Nephrology

Clinical Research Coordinator Surgery

Clinical Research Coordinator Associate

Clinical Research Coordinator (1/2)

Assistant Clinical Research Coordinator

Associate Clinical Education Coordinator

Clinical Research Coordinator (9611C), School of Optometry & Vision Science #87775

Clinical Procurement Coordinator (RRT's, PA's & RN's Preferred)

I want to receive the latest job alert for clinical coordinator in san francisco bay area ca

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