Top 8 Coordinator i Jobs in Honolulu, Hi

Coord I: Clinical Research
Shriners Hospitals for Children —Honolulu, HI
- $26.58 - $39.86 an hour
- Full-time
- 18 years or older
- Hospital
- Bachelor's degree
Quick Apply
6d
Community Program Coordinator I/II (On-site)
Central Pacific Bank —Honolulu, HI
- $20.00 - $29.24 an hour
- Full-time
- Writing skills
- Sanitation
- Mid-level
Quick Apply
DRIVER IMPROVEMENT COORDINATOR I (SR-19) [1 vacancy]
City and County of Honolulu —Honolulu, HI
- $4,933 - $6,003 a month
- Full-time
- Classroom
- Mid-level
- Office
- Health insurance
- Retirement plan
DRIVER IMPROVEMENT COORDINATOR I (SR-19) [1 vacancy]
City and County of Honolulu, HI —Oahu Island, HI
- $4,933 - $6,003 a month
- Full-time
- Classroom
- CDL A
- Mid-level
- Health insurance
- Dental insurance
MAINTENANCE PROJECTS COORDINATOR (WORK PROGRAM COORDINATOR) (SR-22) [1 vacancy]
City and County of Honolulu —Honolulu, HI
- $5,527 - $6,468 a month
- Weekends as needed
- Mid-level
- Health insurance
- Retirement plan
MAINTENANCE PROJECTS COORDINATOR (WORK PROGRAM COORDINATOR) (SR-22) [1 vacancy]
City and County of Honolulu, HI —Oahu Island, HI
- $5,527 - $6,468 a month
- Weekends as needed
- Mid-level
- Analysis skills
- Driver's License
- Health insurance
- Dental insurance
Clinical Donation Coordinator I - PeeDee Region
WE ARE SHARING HOPE SC —United States
- On call
- Mid-level
- Operating room
- 2 years

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Community Program Coordinator I/II (On-site)
Central Pacific Bank —Honolulu, HI
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U.S.Vets Wai'anae —Waianae, HI
Valid driver’s license required, must meet company insurance requirements and complete a provided driver training course.
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Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…

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Coord I: Clinical Research

Shriners Hospitals for Children -
Honolulu, HI

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Job Details

Full-time
$26.58 - $39.86 an hour
6 days ago

Qualifications

Project reporting
CCRC
Clinical study protocols and reports
Informed consent
Presentations for conferences or internal meetings
Research project coordination
Data integrity and documentation
Schedule management
Research report preparation
Records management
Bachelor's degree
Public Health
Data quality monitoring
Informed consent procedures implementation
Clinical trial patient safety management
Implementing research protocols
Patient recruitment
CCRP
Communication with regulatory authorities for clinical trials
Bachelor's degree in public health
Clinical quality assurance standards
1 year
Research participation
Patient data collection
Ethical review application preparation
Research findings presentation
Entry level
FDA regulations
Research compliance audit records management
Research compliance quality assurance records management

Full Job Description

Company Overview

Shriners Children’s is an organization that respects, supports, and values each other. Named as the 2025 best mid-sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.

With 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family’s ability to pay or insurance status. Please click here to learn more about our locations.

Job Description

The Clinical Research Coordinator, Level 1 (CRC I) is a research professional responsible for supporting the oversight and compliance of both system-wide and local Shriners Children’s (SHC) clinical research activities. Reporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and collaborating with the Research Programs Office at SHC International Headquarters, the CRC provides support in accordance with SHC policies and procedures, hospital regulations, the Code of Federal Regulations, and Good Clinical Practice (GCP) guidelines, when applicable.

The CRC works collaboratively with investigators, research staff, and clinical teams to ethically recruit and consent Shriners Children’s vulnerable pediatric research participants and to appropriately collect, manage, and safeguard research data. The CRC serves as a key liaison among research participants, investigators, sponsors, and regulatory bodies to support proper study conduct, subject safety, and the quality and integrity of study data.

Key Responsibilities:

Supports the implementation and conduct of approved research protocols, ensuring studies are performed in compliance with the protocol, Good Clinical Practice (GCP), applicable regulatory requirements, and SHC policies and standards.
Performs study-specific research activities and/or interventions within the bounds of professional licensure and training.
Assists with participant recruitment, screening, informed consent/assent, scheduling, and coordination of study visits.
Coordinates the collection and documentation of research data.
Maintains regulatory documentation and study records in accordance with institutional policies and sponsor requirements.
Supports communication and coordination between investigators, sponsors, monitors, and institutional departments involved in research activities.
Assists investigators with the development and submission of investigator-initiated research protocols and related regulatory documentation.
Contributes to study progress reports, monitoring visits, audits, and preparation of study results or presentations when applicable.
Ensures appropriate training and education are completed in order to safely perform study-related procedures and protocol requirements.

Required Qualifications:

One or more years of relevant research experience, e.g. site management, study management, research regulatory experience, data collection, compliance or other applicable experience.

Preferred Qualifications:

Bachelor’s degree in Clinical Research, Life Sciences, Public Health, or another healthcare-related field
Working knowledge of regulations and guidance related to clinical research (e.g., GCP, FDA regulations, IRB requirements)
Experience coordinating intergroup or multi-site clinical studies
CCRP or CCRC certification
1 or more years of relevant research experience (e.g., study coordination, site management, regulatory submissions, or clinical data management)

The pay range for this position is $26.58 - $39.86. Compensation is determined based on years of relevant experience and departmental equity.

Quick Apply

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coordinator i jobs in honolulu, hi

Coord I: Clinical Research

Community Program Coordinator I/II (On-site)

DRIVER IMPROVEMENT COORDINATOR I (SR-19) [1 vacancy]

DRIVER IMPROVEMENT COORDINATOR I (SR-19) [1 vacancy]

MAINTENANCE PROJECTS COORDINATOR (WORK PROGRAM COORDINATOR) (SR-22) [1 vacancy]

MAINTENANCE PROJECTS COORDINATOR (WORK PROGRAM COORDINATOR) (SR-22) [1 vacancy]

Clinical Donation Coordinator I - PeeDee Region

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