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Research Assistant Iv Jobs in Michigan (NOW HIRING)

4-H Program Assistant

Dewitt, MI · On-site

$31K - $39K/yr

... assistants, need to log in to Workday via MyApps.Microsoft.com, then access Find Jobs from the ... Research and Extension Centers and in every Arkansas county. It consists of the Arkansas ...

4-H Program Assistant

Dewitt, MI

$31K - $39K/yr

... assistants, need to log in to Workday via MyApps.Microsoft.com, then access Find Jobs from the ... Research and Extension Centers and in every Arkansas county. It consists of the Arkansas ...

Showing results 41-60

Research Assistant Iv information

What is a Research Assistant IV?

Research Assistant IVs are advanced-level research staff, typically found in academic or scientific settings, who assist in designing, conducting, and analyzing research projects. They often work under the supervision of principal investigators or faculty and may oversee lower-level research assistants or students. Their duties can include data collection, statistical analysis, literature reviews, and preparing reports or publications. Research Assistant IVs usually have significant experience or advanced education in their field, enabling them to take on more complex research tasks and administrative responsibilities.

What are the key skills and qualifications needed to thrive as a Research Assistant IV?

To thrive as a Research Assistant IV, you typically need advanced research experience, a relevant graduate degree, and strong analytical skills. Familiarity with statistical software (like SPSS or R), laboratory equipment, and research compliance protocols is often required. Exceptional organization, attention to detail, and effective communication skills set candidates apart in this role. These abilities are essential for ensuring the accuracy, integrity, and efficiency of complex research projects.

What are some typical challenges faced by a Research Assistant IV, and how can they be effectively managed?

Research Assistant IVs often encounter challenges such as balancing multiple projects with tight deadlines, managing complex data sets, and adapting to evolving research priorities. Effective time management and strong organizational skills are crucial for staying on top of tasks. Additionally, clear communication with principal investigators and team members helps in prioritizing work and addressing any roadblocks promptly. Embracing collaborative tools and seeking regular feedback can also ensure smoother project progression and professional growth.

What is the difference between Research Assistant Iv vs Research Assistant III?

AspectResearch Assistant IvResearch Assistant III
Required CredentialsBachelor's degree; some roles may prefer master'sBachelor's degree; some roles may prefer master's
Work EnvironmentLaboratories, research facilities, academic institutionsLaboratories, research facilities, academic institutions
Employer & Industry UsageUniversities, government agencies, private research firmsUniversities, government agencies, private research firms
Typical ResponsibilitiesData collection, analysis, assisting senior researchersData collection, analysis, assisting senior researchers, some project management

Research Assistant IV roles generally require similar credentials as Research Assistant III but may involve more complex tasks or specialized knowledge. Both positions are common in academic, government, and private research settings, with the IV level often indicating a higher level of experience or responsibility within the same job family.

What are the most commonly searched types of Research Iv jobs in Michigan?

The most popular types of Research Iv jobs in Michigan are:

What cities in Michigan are hiring for Research Assistant Iv jobs?

Cities in Michigan with the most Research Assistant Iv job openings:

Infographic showing various Research Assistant Iv job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, 2% Temporary, and 3% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution.

Research Associate, Population Sciences - Department of Oncology

Wayne State University

Detroit, MI • On-site

Full-time

Posted 16 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

290th of 622 rated colleges and universities


Job description

Research Associate, Population Sciences - Department of Oncology
Wayne State University is searching for an experienced Research Associate, 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:
We seek a full-time, entry-level Research Associate with a strong foundation in computational genomics and a keen interest in cancer and epidemiology. This role offers the opportunity to contribute to various projectsutilizing -omic data (e.g., GWAS, sequencing, RNA-seq, ATAC-seq) and integrating publicly available datasets from All of Us, UK Biobank, and dbGaP. The focus will be on understanding susceptibility to and survival following hematologic malignancies. This position is an excellent opportunity for someone looking to strengthen their computational skills while developing deeper expertise in cancer genomics and epidemiology. - Under the direction of the PI, design, execute, and interpret genetic studies using diverse quantitative and binary traits from large-scale cohorts. - Collaborate with colleagues in various multi-PI research consortia, including presenting and discussing analysis results. - Stay up to date with advances in human genetic analysis methods and be able to discuss these developments with both experts and non-experts.
Qualifications:
Education: Bachelor's degree
Bachelor's degree from an accredited college or university in public health, psychology, social sciences, nursing, biology, or related fields.
Requires advanced knowledge, predominantly intellectual in character, in a field of science or learning acquired by a prolonged course of specialized intellectual instruction.
Experience: Intermediate (3 to 4 years job-related experience)
Experience conducting clinical or human subjects 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.
Ability to identify workflow issues and recommend process improvements.
Preferred qualifications:
- MS in Statistical Genetics, Human Genetics with Computational Biology, Quantitative Epidemiology, or a relatedfield OR BS with 3+ years of work experience demonstrating an equivalent MS-level understanding of subjectmatter and skill set. - Experience with data QC, analysis, and interpretation of human biological data. Prior experience in human genetics (single variant and gene-based association analysis using WES/WGS/array genotyping data) is ideal, but candidates with relevant experience in adjacent fields and a willingness to learn areencouraged to apply. - Basic understanding of EHR data (e.g., UK Biobank, All of Us) and genomics databases (e.g., gnomAD, 1000 Genomes, TOPMed). Prior hands-on experience with these resources is preferred but not required. - Proficiency in R required; Python is also acceptable. - Working knowledge of Unix/Linux and cloud computing environments. - Strong interest in developing written and verbal communication skills for conveying analysis results to experts and non-experts. - Some experience with peer-reviewed publications and/or conference presentations 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 office, clinical, community, and/or research settings. May require evening or weekend hours to accommodate study participants. May require local travel for recruitment, community engagement, or professional 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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