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Entry Level Irb Analyst Jobs (NOW HIRING)

Research Assistant I/II/III

Columbus, GA · On-site

$17.25 - $23.75/hr

... procedures, and analysis of sleep, otherwise the candidate must be willing to learn these ... Understanding of IRB submissions, amendments, and compliance requirements. * Knowledge of study ...

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Entry Level Irb Analyst information

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$13

$27

$54

How much do entry level irb analyst jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for entry level irb analyst in the United States is $27.77, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $30.05 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Irb Analyst vs Clinical Research Coordinator?

AspectEntry Level Irb AnalystClinical Research Coordinator
Required CredentialsBachelor's degree, familiarity with IRB processesBachelor's degree, experience in clinical trial management
Work EnvironmentOffice-based, regulatory compliance focusClinical sites, patient interaction, trial coordination
Employer & Industry UsageHospitals, research institutions, biotech firmsHospitals, research centers, pharmaceutical companies

While both roles involve clinical research, an Entry Level Irb Analyst primarily focuses on regulatory review and IRB submissions, working in an office setting. In contrast, a Clinical Research Coordinator manages trial logistics and patient interactions at clinical sites. Both roles require a bachelor's degree, but the Coordinator role often demands more direct patient contact and trial management experience.

More about Entry Level Irb Analyst jobs
What cities are hiring for Entry Level Irb Analyst jobs? Cities with the most Entry Level Irb Analyst job openings:
What are the most commonly searched types of Irb Analyst jobs? The most popular types of Irb Analyst jobs are:
Infographic showing various Entry Level Irb Analyst job openings in the United States as of July 2026, with employment types broken down into 40% Full Time, and 60% Part Time. Highlights an 100% In-person job distribution, with an average salary of $57,761 per year, or $27.8 per hour.
Research Assistant, Population Sciences - Department of Oncology

Research Assistant, Population Sciences - Department of Oncology

Wayne State University

Detroit, MI • On-site

$19 - $26.25/hr

Full-time

Posted 6 days ago


Wayne State University rating

7.6

Company rating: 7.6 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

285th of 612 rated colleges and universities


Job description

Research Assistant, Population Sciences - Department of Oncology
Wayne State University is searching for an experienced Research Assistant, Population Sciences - Department of Oncology at its Detroit campus location.
Wayne State is a premier, public, urban research university located in the heart of Detroit, Michigan where students from all backgrounds are offered a rich, high-quality education. Our deep-rooted commitment to excellence, collaboration, integrity, diversity and inclusion creates exceptional educational opportunities which prepare students for success in a global society.
Essential functions (job duties):
Support the design and implementation of clinical research protocols involving human subjects. Recruit and screen study participants through approved methods, including outreach, surveys, and interviews. Conduct study visits and collect clinical and research data in compliance with Institutional Review Board (IRB), regulatory, and protocol requirements. Communicate regularly with the Principal Investigator and research team regarding study progress and participant status.
Collect, enter, and maintain accurate clinical and research data, including outcomes, surveys, and case report forms. Monitor data quality and completeness. Perform preliminary data analysis and generate graphs, charts, and tables to summarize results in accordance with study protocols. Proofread and verify research data and documentation for accuracy.
Prepare and assist with presentations of research findings for professional, scientific, and academic conferences. Organize and summarize study results for submission to peer-reviewed journals. Assist in drafting, factchecking, editing, and proofreading scientific manuscripts, study reports, and regulatory documents.
Maintain organized research records and study files in accordance with regulatory and institutional requirements. Coordinate study materials and supplies, and support documentation for audits, monitoring visits, and regulatory submissions. Ensure workspaces remain organized and compliant with confidentiality and data security standards.
Perform other related duties as assigned.
Unique duties:
- Setting up and running video and audio recording equipment in the exam room in adherence to IRB guidelines
Qualifications:
Education: Bachelor's degree
Bachelor's degree in a related field of study, preferred. Requires advanced knowledge predominantly intellectual in character in a field of science or learning acquired by a prolonged course of specialized intellectual instruction.
Experience: Entry level (less that a year of job-related experience)
Experience conducting clinical or human subject research is preferred. Experience with participant recruitment, informed consent, data collection, and maintenance of regulatory documentation is preferred
Knowledge, Skills and Abilities:
Ability to work independently and manage multiple clinical research activities while adhering to study protocols, regulatory requirements, and timelines. Ability to analyze, summarize, and interpret clinical research data and communicate findings effectively in reports and presentations. Requires knowledge predominantly intellectual in character in a field of science or learning acquired through specialized instruction. Knowledge of scientific integrity principles, responsible conduct of research, and human subject protections (e.g., IRB requirements, confidentiality standards). Excellent time management, organizational, and documentation skills.
Strong interpersonal and communication skills, with demonstrated ability to interact professionally with research participants, clinical staff, and multidisciplinary research teams.
Proficiency in Microsoft Office software (Word, Excel, PowerPoint) and familiarity with clinical research databases or electronic data capture systems is preferred. Ability to recruit and communicate effectively with diverse populations, including medically underserved communities.
Preferred qualifications:
- Bachelor's degree from an accredited college or university in public health, psychology, social sciences, nursing, biology, or related field. -Experience with participant recruitment, informed consent, data collection, and maintenance of regulatory documentation is preferred.
School/College/Division:
H06 - School of Medicine
Primary department:
H0632 - Oncology
Employment type:
  • Regular Employee
  • Job type: Full Time
  • Job category: Research
Funding/salary information:
  • Compensation type: Annual Salary
Working conditions:
Typical work environment may include a laboratory and/ or office environment. May require working non-standard business hoursincluding evenings and weekends. May be required to travel to scientific conferences.
Job openings:
  • Number of openings: 1
  • Reposted position: No
  • Reposted reason: None (New Requisition)
  • Prior posting/requisition number:
Background check requirements:
University policy requires certain persons who are offered employment to undergo a background check, including a criminal history check, before starting work. If you are offered employment, the university will inform you if a background check is required.

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