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Full Time Human Subject Research Jobs (NOW HIRING)

New York University

RESEARCH SCHOLAR

New York, NY · On-site

... Full time Research Scholar to work on exciting projects in signal processing, estimation, control ... human subject research including physiological health data collection * data analysis The ...

New York University

RESEARCH SCHOLAR

New York, NY · On-site

$48K/yr

Description Research Scholar (Full-time) Biomedical Engineering New York University Faculty in the ... human subject research including physiological health data collection and subsequent data analysis.

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Full Time Human Subject Research information

What are the key skills and qualifications needed to thrive in full time human subject research?

To thrive in Full Time Human Subject Research, you need a solid background in scientific methodology, ethical research practices, and often a degree in a relevant field such as psychology, biology, or public health. Familiarity with data collection tools, statistical software (like SPSS or R), and Institutional Review Board (IRB) protocols is typically required. Exceptional attention to detail, strong interpersonal skills, and clear communication help ensure accurate data collection and ethical participant interactions. These skills and qualities are crucial for producing valid research outcomes while safeguarding participant rights and well-being.

What is a full time human subject researcher?

A Full Time Human Subject Researcher is a professional who conducts scientific studies involving human participants. Their work typically includes designing research protocols, recruiting and monitoring subjects, collecting data, and ensuring all research is conducted ethically and in compliance with regulations. They may work in academic, clinical, or private research settings and often collaborate with other scientists and medical professionals. The goal is to advance knowledge in fields such as medicine, psychology, or public health, while prioritizing the safety and rights of human subjects.

What are the typical challenges faced by professionals in full time human subject research roles?

Professionals working in full-time human subject research often face challenges such as recruiting and retaining participants, ensuring strict compliance with ethical guidelines and institutional review board (IRB) protocols, and managing sensitive data securely. Balancing administrative tasks with hands-on research activities can also be demanding, as can coordinating with multidisciplinary teams including clinicians, statisticians, and regulatory staff. Strong organizational skills and adaptability are key to successfully navigating these complexities while maintaining the integrity of the study.

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

AspectFull Time Human Subject ResearchFull Time Clinical Research Coordinator
CredentialsOften requires a bachelor's degree in health sciences, psychology, or related fields; certifications like CITI are commonTypically requires a bachelor's degree; certifications like CITI or CCRP are advantageous
Work EnvironmentResearch institutions, universities, hospitals conducting human subject studiesClinical trial sites, hospitals, research centers managing patient studies
Employer & IndustryAcademic, government, or private research organizationsPharmaceutical companies, hospitals, clinical research organizations

Both roles involve working with human subjects in research settings, but Full Time Human Subject Research often focuses on designing and analyzing studies, while Clinical Research Coordinators manage day-to-day trial operations. Understanding these differences helps job seekers identify the right career path in clinical research.

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What are the most commonly searched types of Human Subject Research jobs? The most popular types of Human Subject Research jobs are:
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What job categories do people searching Full Time Human Subject Research jobs look for? The top searched job categories for Full Time Human Subject Research jobs are:
Full Time Human Subject Research jobs near you
Infographic showing various Full Time Human Subject Research job openings in the United States as of August 2026, with employment types broken down into 55% Full Time, 27% Part Time, 1% Temporary, and 17% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

Clinical Research Coordinator II

University of Massachusetts Medical School

Worcester, MA • Remote

$23.08 - $27.88/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

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.


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

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