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Full Time Disability Research Jobs (NOW HIRING)

Headlands Research

Clinical Research Coordinator

Lake Worth, FL · On-site

$21.50 - $28.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

JEM Research Institute | Full-Time Are you an experienced clinical research professional with a ... of disability, accident, and life insurance options, as well as many more. What We Offer

Headlands Research

Clinical Research Coordinator II

San Diego, CA · On-site

$25.75 - $34.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We offer the following generous benefits to our full-time employees: * A range of PPO and HMO ... Vision coverage, long term disability plan, and life/AD&D coverage * 401k plan * Paid holidays and ...

Obiter Research

Research Chemistry Manager

Champaign, IL · On-site

$73K - $81K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Employee sponsored benefits including Short Term Disability and Life Insurance * 401(k) Retirement ... Job Type: Full-time Pay: $73,400.00 - $81,200.00 per year Benefits: * 401(k) * 401(k) matching

Alcanza Clinical Research

Research Assistant

Birmingham, AL · On-site

$18 - $24.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Operations Employment Type: Full Time Location: Accel Research Sites - Birmingham, AL Reporting To ... Medical, dental, vision, life insurance, short and long-term disability insurance, health savings ...

Obiter Research

Research Chemistry Manager

Champaign, IL · On-site

$73K - $81K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Employee sponsored benefits including Short Term Disability and Life Insurance * 401(k) Retirement ... Job Type: Full-time Pay: $73,400.00 - $81,200.00 per year Benefits: * 401(k) * 401(k) matching

Obiter Research

Research Chemistry Manager

Champaign, IL · On-site

$73K - $81K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Employee sponsored benefits including Short Term Disability and Life Insurance * 401(k) Retirement ... Job Type: Full-time Pay: $73,400.00 - $81,200.00 per year Benefits: * 401(k) * 401(k) matching

Headlands Research

Senior Clinical Research Coordinator

Portland, OR · On-site

$25.75 - $34.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Summit Research Network | Full-Time | Clinical Research Are you an experienced clinical research ... of disability, accident, and life insurance options, as well as many more. What We Offer

Headlands Research

Clinical Research Coordinator III

San Diego, CA · On-site

$70K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We offer the following generous benefits to our full-time employees: * A range of PPO and HMO ... Vision coverage, long term disability plan, and life/AD&D coverage * 401k plan * Paid holidays and ...

Flourish Research

Clinical Research Coordinator

Walnut Creek, CA · On-site

$24 - $33/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Shift: Full time, Monday-Friday, 8:30 - 5 PM (flexibility needed depending on patient schedules ... disability insurance, and 15 days of PTO + 8 paid holidays and 2 floating holidays. Flourish ...

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Showing results 21-40

All Jobsdisability research Jobsfull time JobsFull Time Disability Research Jobs

Full Time Disability Research information

What is a full time disability researcher?

A Full Time Disability Researcher is a professional who conducts studies and analysis focused on disability-related topics, such as accessibility, inclusion, and the impact of disabilities on individuals and communities. They may work in academic, government, or nonprofit settings, and their work often involves designing research projects, collecting and analyzing data, and publishing findings. The goal is to improve understanding of disabilities and inform policy or social services. Full time researchers typically dedicate their entire work schedule to these activities and may also collaborate with advocacy groups or participate in developing new programs.

What are the key skills and qualifications needed to thrive as a full time disability researcher, and why are they important?

To thrive as a Full Time Disability Researcher, a strong background in social sciences, public health, or disability studies—often at the graduate level—is typically required. Familiarity with research methodologies, data analysis software (such as SPSS or NVivo), and ethical research practices is essential. Excellent communication, empathy, and critical thinking skills help researchers engage with diverse populations and interpret complex findings. These skills ensure rigorous, ethical research that contributes meaningfully to the understanding and improvement of disability-related issues.

What are some common challenges faced by professionals in full time disability research roles, and how can they be addressed?

Professionals in full-time disability research often encounter challenges such as recruiting and retaining diverse participants, navigating complex ethical considerations, and ensuring accessibility in both research methods and dissemination. These can be addressed by building strong partnerships with disability communities, maintaining rigorous informed consent procedures, and utilizing accessible formats for surveys, interviews, and reporting. Collaboration with stakeholders and ongoing professional development in disability studies can also help researchers stay updated on best practices and inclusive methodologies.

What is the difference between Full Time Disability Research vs Part Time Disability Research?

AspectFull Time Disability ResearchPart Time Disability Research
Work HoursTypically 35-40 hours per weekLess than 20 hours per week
CredentialsRequires similar qualifications, such as a master's or PhD in related fieldsSame credentials as full-time roles
Work EnvironmentResearch labs, offices, or clinical settingsFlexible, often remote or part-time settings
Employer UsageUsed by research institutions, healthcare organizations, and universitiesUsed by similar employers offering flexible roles

Full Time Disability Research involves working standard hours with comprehensive responsibilities, while Part Time Disability Research offers flexible schedules with similar qualifications. Both roles focus on disability studies but differ mainly in hours and work setup.

More about Full Time Disability Research jobs

What cities are hiring for Full Time Disability Research jobs?

Cities with the most Full Time Disability Research job openings:

What are the most commonly searched types of Disability Research jobs?

The most popular types of Disability Research jobs are:

What states have the most Full Time Disability Research jobs?

States with the most job openings for Full Time Disability Research jobs include:

What job categories do people searching Full Time Disability Research jobs look for?

The top searched job categories for Full Time Disability Research jobs are:

Full Time Disability Research jobs near you
Infographic showing various Full Time Disability Research job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 3% Contract, and 1% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution.

Clinical Research Coordinator

Headlands Research

Lake Worth, FL • On-site

$21.50 - $28.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 days ago

Job description

Clinical Research Coordinator (CRC)

Location: Lake Worth, FL | Site Name: JEM Research Institute | Full-Time

Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.

We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Lake Worth, FL. The CRC will manage and execute Phase II-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.

Type:  Regular Full-time Employee
Schedule:  Mondays through Fridays, 8:30am - 4:30pm
Location:  Onsite in Lake Worth, FL (no capabilities for remote or hybrid work)
Reports to:  Clinical Research Manager
Benefits:  Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • A mission-driven culture focused on advancing medicine and improving patient outcomes
 Why Join Us?

You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.

Responsibilities:

  • Coordinate all aspects of assigned clinical trials from site initiation to study close-out
  • Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards
  • Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs
  • Manage subject recruitment, informed consent, and retention strategies
  • Ensure timely data entry and resolution of EDC queries
  • Report and follow up on all adverse events, serious adverse events, and deviations
  • Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems
  • Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control

Requirements:

  • Required: High school diploma or GED
  • Experience:
    • Minimum of 1 year of experience as a Clinical Research Coordinator OR
    • Minimum of 2 years of experience as a Research Assistant in Clinical Research
  • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
  • Proficiency in medical terminology and clinical documentation practices
  • Strong interpersonal, verbal, and written communication skills
  • Organized, detail-oriented, and capable of managing multiple priorities
  • Proficient in Microsoft Office and other clinical research systems
  • Bilingual (English/Spanish) is strongly preferred

Apply now to become a part of a team that's changing the future of healthcare-one trial at a time.

Apply