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Research Study Assistant Jobs (NOW HIRING)

Dartmouth College

Research Assistant I

Hanover, NH · On-site

$19.25 - $26.50/hr

This candidate chosen for this position will perform a wide variety of research study/office ... The Research Assistant will assist with procedures related to the collection, tracking, storage ...

Dartmouth College

Research Assistant I

Hanover, NH · On-site

$19.25 - $26.50/hr

This candidate chosen for this position will perform a wide variety of research study/office ... The Research Assistant will assist with procedures related to the collection, tracking, storage ...

Horizon Clinical Research

Be Seen First

Clinical Research Assistant

Cypress, TX · On-site

$37K - $47K/yr

We are seeking an experienced and detail oriented Clinical Research Assistant (CRA) for our Cypress ... Recruits patients for clinical research studies based on study inclusion/exclusion. * Obtains ...

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How much do research study assistant jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for research study assistant in the United States is $21.91, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $25.48 per hour, depending on experience, location, and employer.

How much does a research study assistant get paid?

Research study assistants typically earn between $12 and $20 per hour, depending on experience, location, and the complexity of the research. Some positions may offer additional benefits or stipends, especially in academic or clinical settings.

Is it hard to get a job as a research study assistant?

Securing a position as a research study assistant typically requires relevant education, such as a bachelor's degree in a related field, and sometimes prior experience or familiarity with research tools like data analysis software. Competition can vary depending on the institution and location, but strong organizational skills and attention to detail are often valued by employers.

What are the key skills and qualifications needed to thrive as a research study assistant?

To thrive as a Research Study Assistant, you need a solid understanding of research methods, data collection, and basic statistical analysis, often supported by a bachelor's degree in a relevant field. Familiarity with data management software (such as REDCap or SPSS) and compliance with research ethics certifications are typical requirements. Attention to detail, strong organizational abilities, and effective communication skills are vital soft skills for this role. These competencies ensure accurate data handling, adherence to protocols, and successful collaboration with research teams.

What is the difference between Research Study Assistant vs Research Coordinator?

AspectResearch Study AssistantResearch Coordinator
CredentialsTypically requires a bachelor's degree in a related fieldOften requires a bachelor's degree; some roles prefer or require additional certifications
Work EnvironmentAssists with data collection, participant recruitment, and administrative tasks in research settingsOversees study protocols, manages staff, and ensures compliance in research projects
Employer & IndustryHospitals, universities, research institutesHospitals, research organizations, academic institutions

The main difference is that Research Study Assistants support data collection and administrative tasks, while Research Coordinators manage study operations and oversee research projects. Both roles are essential in research settings but differ in responsibilities and level of oversight.

What is a research study assistant?

Research Study Assistants are professionals who support the design, implementation, and management of research studies, often in academic, medical, or scientific settings. Their responsibilities typically include recruiting participants, collecting and organizing data, maintaining study records, and ensuring compliance with research protocols. They work closely with principal investigators and other research staff to ensure studies run smoothly and efficiently. Research Study Assistants play a crucial role in maintaining data integrity and supporting the overall success of research projects.

What are some typical challenges research study assistants face when coordinating participant recruitment and data collection?

Research Study Assistants often encounter challenges such as recruiting enough qualified participants within tight timelines and maintaining participant engagement throughout the study. Managing scheduling conflicts, ensuring informed consent, and adhering to strict data collection protocols are also common hurdles. Successful assistants are proactive in communication, detail-oriented, and adept at troubleshooting unexpected issues that may arise during recruitment or data gathering. Building rapport with participants and collaborating closely with the research team helps address these challenges effectively.
More about Research Study Assistant jobs
What cities are hiring for Research Study Assistant jobs? Cities with the most Research Study Assistant job openings:
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Research Study Assistant jobs near you
Infographic showing various Research Study Assistant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 21% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $45,571 per year, or $21.9 per hour.

Research Study Coordinator-Research Center (Knoxville)

The University of Tennessee

Knoxville, TN • On-site

$21.69/hr

Full-time

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

Job description


Market Range: 08
Hiring Range: $21.69/Hourly
THIS IS A TWO YEAR GRANT-FUNDED POSITION LOCATED IN KNOXVILLE, TN.
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under the direction of the GSM Director of Research, the Research Study Coordinator 1 performs as the Research Study Coordinator for Investigator-Initiated Research. This position assists the faculty with clinical research study activities including but not limited to the development, submission and management of regulatory paperwork, the submission of Institutional Review Board (IRB) applications and annual renewals, and preparation and maintenance of study files and essential trial documents.
Responsibilities
  1. Assists investigators with the development of design studies by reviewing proposals to determine best-suited methods for study objectives.
  2. Assist investigators with the collection and submission process for initial Institutional Review Board (IRB) submissions including the collection of hospital collaboration agreements, key personnel documents, department approvals, funding source information, Investigational New Drug (IND) information, Drug(s)/Device(s) specifics, and IRB application completion and upload into iMedRIS.
  3. Assists investigator with the IRB Continuing Review process that includes the completion of study status reports.
  4. Prepares study-specific protocols, source documents/spreadsheets, drafts of required study logs and essential trial documents, and prepares files.
  5. Assists investigator with the execution and coordination of GSM Investigator-Initiated Research.
  6. Assists in screening potential subjects, reviewing and documenting patient medical histories and concurrent medication lists, obtaining informed consent from patients, coordinating study visits and procedures to be completed on campus, collecting study data, and performing study assessments if needed (lab draws, questionnaires, vital signs, etc.) for Investigator-Initiated Studies.
  7. Establishes and maintains contact with study participants and families, community agencies, and health care providers.
  8. Assists investigator with the management and maintenance of study specific Master Trial File and Essential Trial Documents.
  9. Assists investigators and the Director of Research with the coordination of Quality Assurance and Monitoring pathway audits.
  10. Performs other duties assigned.

Qualifications
EDUCATION: Bachelor's Degree in relevant health field. (TRANSCRIPT REQUIRED)
EXPERIENCE: One (1) year of relevant experience; OR Associate's Degree and three (3) years of relevant experience, OR an equivalent combination of education, training, and experience to equal five (5) years.
KNOWLEDGE, SKILLS, AND ABILITIES:
  • Ability to create and maintain extensive medical records on clinical research subjects.
  • Understanding of hospital policies and procedures, medical records and documentation, and HIPAA regulations.
  • Knowledge of research protocol with an understanding of Basic Research Principles and Federal Code of Regulations for Clinical Research Studies.
  • Ability to manage multiple priorities.
  • Ability to interact with a diverse population.
  • Intermediate-level computer skills with the ability to learn new software applications for various electronic data capture programs.
  • Ability to exhibit strong interpersonal and communication skills.

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