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Remote Human Subject Research Jobs (NOW HIRING)

University of Rochester

Project Coordinator

New York, NY · On-site +1

$21.36 - $29.90/hr

Remote Work - New York, Albany, New York, United States of America, 12224 Opening: Worker Subtype ... Coordinates the activities associated with human subject research. ESSENTIAL FUNCTIONS

Georgetown University

IRB Analyst

Washington, DC · On-site +1

$47K - $87K/yr

The Office of Human Subject Protections reports to the Medical Center Dean for Research and the ... Remote . Please note that work mode designations are regularly reviewed in order to meet the ...

Genstar Capital LLC

$50K - $66K/yr

S. and/or Canadian Regulations and Guidelines in Human Subject Protections, drug research, device research, and cosmetic research * Completing standard Human Subjects Research Training, such as CITI ...

Advarra

Editor I, Consent Form Development

$50K - $66K/yr

S. and/or Canadian Regulations and Guidelines in Human Subject Protections, drug research, device research, and cosmetic research * Completing standard Human Subjects Research Training, such as CITI ...

Gonzalez MD and Aswad MD Health

Be Seen First

Clinical Research PhD- sub - investigator / PI Track

Miami, FL · Remote

$500 - $1K/day

Strong understanding of GCP, FDA regulations, human subject protection, and research documentation standards * Strong communication, organizational, and leadership skills * Ability to work ...

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Remote Human Subject Research information

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How much do remote human subject research jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for remote human subject research in the United States is $23.39, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $28.37 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Remote Human Subject Research, and why are they important?

To excel in Remote Human Subject Research, you need a solid understanding of research methodologies, ethical guidelines, and data analysis, often supported by a relevant degree in psychology, social sciences, or a related field. Familiarity with online survey platforms, remote interview tools, and compliance systems such as IRB protocols is typically required. Excellent communication, attention to detail, and organizational skills help researchers manage participant interactions and data integrity remotely. These competencies are crucial for ensuring valid, ethical, and efficient research while maintaining participant trust and data quality in a virtual environment.

What is the difference between Remote Human Subject Research vs Remote Clinical Research Coordinator?

AspectRemote Human Subject ResearchRemote Clinical Research Coordinator
CredentialsTypically requires a background in health sciences, psychology, or related fields; certifications like IRB training may be preferredRequires similar health sciences background; often certified in Good Clinical Practice (GCP) or Clinical Research Certification
Work EnvironmentPrimarily conducts studies involving human participants remotely, including data collection and analysisCoordinates clinical trials remotely, managing study protocols, participant recruitment, and data management
Industry UsageUsed in academic, healthcare, and research institutions focusing on human behavior and health studiesCommon in pharmaceutical, biotech, and healthcare industries managing clinical trial processes

Remote Human Subject Research and Remote Clinical Research Coordinators both work with human participants and require health-related credentials. However, Human Subject Researchers focus on designing and analyzing studies involving participants, while Clinical Research Coordinators manage the logistics and compliance of clinical trials. Both roles are essential in advancing health research remotely, but their specific responsibilities differ.

What are some common challenges faced by remote human subject researchers, and how can they be addressed?

Remote human subject researchers often encounter challenges such as ensuring participant engagement, maintaining data security, and navigating technical issues during virtual interactions. To overcome these, researchers should utilize secure, user-friendly platforms for data collection, provide clear instructions and support to participants, and implement robust protocols for informed consent and confidentiality. Regular communication and flexibility in scheduling can also help foster participant trust and increase retention throughout the study.

What is remote human subject research?

Remote human subject research refers to studies or experiments involving people as participants, where all or most activities are conducted online or outside of traditional in-person settings. This can include surveys, interviews, behavioral studies, or clinical trials carried out using digital platforms, video calls, or wearable devices. Remote research allows for greater flexibility, broader participant recruitment, and often improved convenience for both researchers and participants. However, it also requires careful attention to privacy, informed consent, and data security.
More about Remote Human Subject Research jobs
What cities are hiring for Remote Human Subject Research jobs? Cities with the most Remote Human Subject Research job openings:
What are the most commonly searched types of Human Subject Research jobs? The most popular types of Human Subject Research jobs are:
What states have the most Remote Human Subject Research jobs? States with the most job openings for Remote Human Subject Research jobs include:
What job categories do people searching Remote Human Subject Research jobs look for? The top searched job categories for Remote Human Subject Research jobs are:
Remote Human Subject Research jobs near you
Infographic showing various Remote Human Subject Research job openings in the United States as of May 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Temporary. Highlights an 100% Remote job distribution, with an average salary of $48,647 per year, or $23.4 per hour.
Clinical Research Coordinator II

Clinical Research Coordinator II

University of Massachusetts Medical School

Worcester, MA • On-site, Remote

$48K - $55K/yr

Full-time

Posted 26 days ago

Job description

POSITION SUMMARY:

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator II is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for complex research protocols related to treatment, ancillary services, and prevention practices.

Our research team conducts an array of studies related to addressing social disparities and perinatal and pediatric care. We work with directly with families with social disadvantage, including families with limited English proficiency, families of minoritized race/ethnicity, and those with low-income.  We do an array of clinical and health services research using qualitative and quantitative methods. We do observational and interventional studies. We are seeking a Clinical Research Coordinator to join our growing, passionate research team and work under the direction of the Principal Investigator (PI) or designee. Tasks will involve a large array of procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary services, and prevention practices. Our team is seeking a highly motivated individual with an interest in social determinants of health and addressing disparities in healthcare.


ESSENTIAL FUNCTIONS:

  • Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA
  • Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls
  • Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data
  • Conduct preliminary quality assurance reviews of study data
  • Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe
  • Present study status reports related to assigned research projects
  • Contribute to data presentations and Institutional Review Board (IRB) processes
  • Track and maintain study related information in the data management system within the required timeframe Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs
  • Contribute to the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • Responsible for monitoring the inventory of research related supplies
  • Document and collect data/ samples for research related procedures performed during participant study visits. Ensure clinicians and/or PI accurately document their study activities according to protocol.
  • Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
  • Comply with all safety and infection control standards appropriate to this position
  • Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices Perform other duties as required.

REQUIRED QUALIFICATIONS:

  • Bachelor’s degree in a scientific or health related field, or equivalent experience
  • 1-3 years of related experience
  • Ability to travel off site locations

Fluent in Spanish preferred 


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