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Disability Research Jobs in Silver Spring, MD (NOW HIRING)

Clinical Research Coordinator

Vienna, VA

$24.25 - $32.25/hr

Why DelRicht Research? Would you love to be a part of the cutting edge of healthcare and science ... Short and Long Term Disability and Group Life Coverage * Paid Time Off that builds throughout your ...

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

Job Title Research Nurse Concentric Methods is seeking a Research Nurse to join our team in ... disability insurance, tuition reimbursement, as well as 401K with company match. This job will be ...

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

Job Title Research Nurse Concentric Methods is seeking a Research Nurse to join our team in ... disability insurance, tuition reimbursement, as well as 401K with company match. This job will be ...

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

... disability insurance, tuition reimbursement, as well as 401K with company match. This job will be ... Knowledge of clinical research data collection and clinical data report preparation. Working ...

Research Physicist

Washington, DC · On-site

$145K - $185K/yr

Seeking a highly motivated and skilled Research Physicist with a strong background in optics to ... Benefits: Medical, Dental, & Vision Plan, short- and long-term disability, accidental death ...

Job Title Research Nurse Concentric Methods is seeking an experienced Research Nurse to ... disability insurance, tuition reimbursement, as well as 401K with company match. This job will be ...

Concentric Methods is seeking an experienced Research Nurse to independently provide support ... disability insurance, tuition reimbursement, as well as 401K with company match. This job will be ...

We are currently searching for a Research Nurse to support clinical research through participant ... Short-Term & Long-Term Disability * Tuition Reimbursement, Personal Development, Certifications ...

Research Nurse

Rockville, MD · On-site

$98K - $163K/yr

We are currently searching for a Research Nurse to support clinical research through participant ... Short-Term & Long-Term Disability * Tuition Reimbursement, Personal Development, Certifications ...

Research Analyst

Arlington, VA · On-site

$200K - $250K/yr

Research Analyst sought by Sands Capital Management, LLC in Arlington, VA. 40 hrs./wk. Hybrid ... religion, disability status, gender, sexual orientation, gender identity, genetic information ...

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Disability Research information

See Silver Spring, MD salary details

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How much do disability research jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for disability research in Silver Spring, MD is $30.71, according to ZipRecruiter salary data. Most workers in this role earn between $18.44 and $37.12 per hour, depending on experience, location, and employer.

What are some typical daily responsibilities for someone working in disability research?

As a professional in Disability Research, your daily responsibilities often include designing and conducting studies, analyzing survey data, and reviewing relevant literature. You may also collaborate with interdisciplinary teams, interview research participants, and prepare detailed reports or presentations of your findings. Additionally, you’ll frequently engage with stakeholders such as policymakers, advocacy groups, and people with disabilities to ensure your research addresses real-world needs. This role requires a mix of independent research and teamwork, as well as adaptability to shifting project priorities.

What is a disability research?

A Disability Research job involves studying various aspects of disabilities, including their causes, effects, policies, and support systems. Researchers in this field analyze data, conduct surveys, and evaluate programs to improve accessibility, inclusion, and quality of life for individuals with disabilities. They may work in academic institutions, government agencies, nonprofits, or healthcare organizations. The goal is to inform policy, develop interventions, and promote equal opportunities for people with disabilities.

What are the key skills and qualifications needed to thrive in disability research, and why are they important?

To thrive in Disability Research, you need strong analytical skills, a background in social sciences or public health, and experience with research methodologies, often supported by an advanced degree. Familiarity with data analysis software such as SPSS or NVivo and knowledge of accessibility standards are typically required, with certifications in human subjects research being advantageous. Excellent communication, empathy, and cultural competence are vital soft skills for engaging diverse populations and presenting findings effectively. These skills are crucial to conducting ethical research, producing meaningful insights, and advancing inclusion for people with disabilities.

What job categories do people searching Disability Research jobs in Silver Spring, MD look for? The top searched job categories for Disability Research jobs in Silver Spring, MD are:
Infographic showing various Disability Research job openings in Silver Spring, MD as of July 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 90% In-person, and 10% Remote job distribution, with an average salary of $63,869 per year, or $30.7 per hour.

Clinical Research Coordinator

Headlands Research

Baltimore, MD • On-site

$24 - $32/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 29 days ago


Job description

Clinical Research Coordinator (CRC)

Location: Pikesville, MD | Site Name: Headlands Research - Pharmasite | 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 Pikesville, MD. The CRC will manage and execute Phase I-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, 8:00am - 5:00pm
Location:  Onsite in Pikesville, MD (no capabilities for remote or hybrid work)
Reports to:  Site Director
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:

  • Bachelor's degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required OR licensed as a Licensed Practical Nurse (LPN) or higher
  • Previous experience as a Clinical Research Coordinator preferred
  • 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

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