Top 16177 Study coordinator Jobs

Part-Time Study Coordinator
Aperia Medical —Livonia, MI
- $20 an hour
- Part-time
- Hybrid work
- Background check
- Engineering
- HIPAA
- Flexible schedule
Quick Apply
Clinical Research Coordinator (2+ Years Exp required)
Bioresearch Partner —Miami, FL
- $27 - $33 an hour
- Full-time
- Spanish
- Blood sampling
- Vital signs
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator III
Vanderbilt University Medical Center —Nashville, TN
- Full-time
- Hybrid work
- Spanish
- Bachelor's degree
- Continuous improvement
- Health insurance
Study Coordinator
Procom —Chapel Hill, NC
- Contract
- Mid-level
- Office
- University
Quick Apply
7d
Clinical Research Coordinator
The Plastic Surgery Center —Glen Rock, NJ
- $55,000 - $65,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- In-person
- Profit sharing
- Mileage reimbursement
Quick Apply
Preclinical Study Coordinator
Neuralink —Austin, TX
- $31 - $53 an hour
- Full-time
- Master's degree
- Bachelor's degree
- 1 year
- Commuter assistance
- Paid holidays
Study Coordinator
Howard University —Washington, DC
- $50,000 - $60,000 a year
- Full-time
- Word processing
- Bachelor of Science
- English
- 403(b) matching
- Commuter assistance
Associate Clinical Research Coordinator
University of North Carolina at Chapel Hill —Chapel Hill, NC
- $50,312 - $57,000 a year
- Full-time
- Mid-level
- University
- Bachelor's degree
- Health insurance
- Retirement plan
13d
Study Coordinator
North American Science Associates, LLC. —Northwood, OH
- Full-time
- Bachelor of Science
- Pass drug screening
- Office
Quick Apply
12d
Study Coordinator
Hematogenix Laboratory Sv —Tinley Park, IL
- Full-time
- Bachelor of Science
- Writing skills
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Study Coordinator
INOTIV BOULDER LLC —Boulder, CO
- $27 - $34 an hour
- Overtime
- Microsoft Outlook
- Mid-level
- Math
- Paid parental leave
- Disability insurance
Quick Apply
Biospecimen Coordinator
University of North Carolina at Chapel Hill —Chapel Hill, NC
- $59,566 - $70,972 a year
- Overtime
- Mid-level
- Databases
- Bachelor's degree
- Health insurance
- Retirement plan
6d
Study Coordinator
Frontage Laboratories —Chicago, IL
- $21.64 - $26.45 an hour
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
7d
Study Coordinator
Rocky Mountain Cancer Centers —Denver, CO
- $60,000 - $75,000 a year
- Background check
- Pass drug screening
- Mid-level
- Wellness program
- Health savings account
Clinical Research Coordinator (Charlotte, NC)
SiteBridge Research, Inc. —Charlotte, NC
- $30 - $36 an hour
- Part-time
- Spanish
- Mid-level
- 3 years
Quick Apply
Remote Site Manager
IntraCare Health Center —Remote
- Part-time
- Remote
- Mid-level
- Travel
- Leadership
Quick Apply
5d
Clinical Research Regulatory Coordinator (Brandon, Florida)
Cardiovascular Associates of America —Brandon, FL
- Full-time
- Remote
- Mid-level
- Continuous improvement
- Associate's degree
Quick Apply
14d
Senior Study Coordinator
Meso Scale Diagnostics, LLC. —Gaithersburg, MD
- $67,900 - $101,000 a year
- Mid-level
- Office
- Master's degree
- Paid parental leave
- AD&D insurance
Quick Apply
Central Study Coordinator- Retention
Care Access —Boston, MA
- $65,000 - $75,000 a year
- Remote
- Spanish
- Computer literacy
- Writing skills
- Health savings account
- Paid holidays
R-112413 Clinical Research Recruitment Coordinator
Carbon Health Technologies Inc —California
- $0 a year
- Part-time
- Remote
- Mid-level
- Fair chance
- Health savings account
- Disability insurance
Quick Apply

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Part-Time Study Coordinator

Aperia Medical
Livonia, MI

Quick Apply

Job Details

Part-time | Contract
$20 an hour

Benefits

Flexible schedule

Qualifications

Teamwork
Clinical research
Informed consent
Research ethical considerations
HIPAA
Attention to detail
Project management experience in healthcare
Informed consent procedures implementation
Health information regulatory compliance
Organizational skills
Managing projects
Research regulatory compliance
Good Clinical Practice (GCP)
Clinical confidentiality policies
Research and development project management
Associate's degree
Medical terminology
FDA regulations

Full Job Description

About Aperia

Aperia Medical is a health technology company developing AI-based software for breast ultrasound imaging. Our tools are designed to improve detection of breast cancer by helping radiologists find suspicious lesions earlier and characterize them more accurately. The deep learning models we develop are trained and validated on ultrasound exam images that we collect from local patient volunteers, referred to us by surrounding hospitals and partner care providers.

Overview

Aperia Medical is seeking a detail-oriented Study Coordinator to manage day-to-day project operations on a part-time basis. This role is central to our ultrasound case accrual efforts, regulatory compliance, and data quality as we expand our clinical evidence base.

We are seeking a dedicated Part-Time Study Coordinator to support subject recruitment and data collection efforts in Livonia, MI. This vital role involves managing and coordinating our IRB-approved engineering studies and supporting the overall success of our product development projects. As a Study Coordinator, you will play a key role in facilitating smooth operations of our clinical case collection initiatives within a cross-functional team of subject matter experts. This position offers an exciting opportunity for individuals passionate about clinical research and healthcare compliance to make a meaningful impact while working flexible hours.

Responsibilities

Serve as a primary point of contact and liaison with referral sites, potential participants, enrolled subjects, and project staff.
Oversee the recruitment, screening, and enrollment of study participants in accordance with protocol guidelines.
Track and report on case accrual metrics, flagging enrollment gaps or risks to study timelines.
Maintain accurate, audit-ready records of consent, eligibility, and case-level data in compliance with HIPAA and applicable regulations.
Coordinate study activities, including scheduling participant visits, collecting data, and ensuring adherence to study timelines.
Review and verify clinical documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards.
Monitor participant progress through data collection, medical records verification, and follow-up on clinical outcomes.
Maintain detailed records of study activities and ensure data integrity.
Ensure strict compliance with healthcare regulations such as HIPAA and healthcare ethical guidelines throughout all study processes.
Perform protocol procedures, such as automated tomographic breast ultrasound (ATBUS) image acquisition on eligible volunteers who have provided written informed consent to participate in the case collection study.

Experience

Associate's degree or equivalent experience relevant to life sciences, public health, clinical research, or related field
2+ years of experience in clinical research coordination, preferably in medical imaging, oncology, or medical device/diagnostics settings.
Working knowledge of IRB processes, informed consent procedures, and human subjects research regulations (45 CFR 46, HIPAA).
Excellent written and verbal communication skills for coordinating across clinical and technical teams
Knowledge of medical terminology, clinical laboratory procedures, and data management practices.
Familiarity with FDA regulations, ICH GCP guidelines, and HIPAA compliance standards.
Strong organizational skills with project management experience in clinical development or research settings are essential to succeed in this position.

Preferred

Bachelor's degree relevant to life sciences, public health, clinical research, or related field
Supervising experience in clinical research or healthcare settings
Proven management of clinical trials or research projects within a healthcare or laboratory environment.
Certification in ICH GCP (Good Clinical Practice) from a recognized training program
Background in nursing or experience working as a medical imaging technologist

Pay: $20.00 per hour

Benefits:

Flexible schedule

Application Question(s):

While this is a hybrid position, working mostly from home, will you be able to reliably commute to Livonia, MI 48154, as needed, for certain on-site responsibilities of this job?
Do you have the minimum skillset and experience to compliantly work in a clinical study coordinator role, undertaking the standard responsibilities, and adhering to ICH GCP and federal research regulations?
Do you understand and accept that this part-time position is paid hourly, without any additional benefits?
What aspects of this job opportunity motivated you to apply and why?

Education:

Associate (Required)

Experience:

Clinical research: 2 years (Required)

Ability to Commute:

Livonia, MI 48154 (Required)

Work Location: Hybrid remote in Livonia, MI 48154

Quick Apply

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