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Associate Clinical Scientist Jobs in Michigan (NOW HIRING)

Natera

$110K - $130K/yr

The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... scientists, business professionals, software engineers and many other professionals from world ...

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Merck

The associate CRM could be responsible for a particular study for a country or a cluster ... Scientific and clinical research knowledge is required. * Understanding of clinical trial planning ...

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Associate Clinical Scientist information

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$24

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$71

How much do associate clinical scientist jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for associate clinical scientist in Michigan is $47.72, according to ZipRecruiter salary data. Most workers in this role earn between $35.00 and $59.52 per hour, depending on experience, location, and employer.

What is an associate clinical scientist?

Associate Clinical Scientists are professionals who support the design, implementation, and monitoring of clinical trials and research studies in healthcare and pharmaceutical settings. They work closely with clinical teams to ensure that studies comply with regulatory requirements and scientific standards. Their responsibilities may include collecting and analyzing data, preparing reports, and assisting with protocol development. Typically, they have a background in life sciences and are involved in advancing medical research and improving patient care.

How does an associate clinical scientist typically collaborate with cross-functional teams during a clinical trial?

As an Associate Clinical Scientist, you will regularly work with multidisciplinary teams including clinical operations, data management, regulatory affairs, and biostatistics. Your role often involves supporting the design and execution of clinical studies, ensuring protocols are followed, and communicating scientific findings. Effective collaboration is key, as you may participate in team meetings, contribute to study documentation, and help resolve study-related issues. This collaborative environment fosters learning from experienced colleagues and provides a well-rounded view of the clinical development process.

What are the key skills and qualifications needed to thrive as an associate clinical scientist, and why are they important?

To thrive as an Associate Clinical Scientist, you need a solid foundation in biological sciences, analytical skills, and usually at least a bachelor's degree in a relevant field. Familiarity with laboratory information management systems (LIMS), statistical analysis tools, and regulatory standards such as GLP or GCP is typically expected. Strong attention to detail, teamwork, and effective written and verbal communication set exceptional candidates apart. These competencies ensure accurate data collection, regulatory compliance, and effective collaboration in clinical research environments.

What is the difference between Associate Clinical Scientist vs Clinical Research Associate?

AspectAssociate Clinical ScientistClinical Research Associate
Required CredentialsBachelor's or Master's in life sciences, relevant certificationsBachelor's in life sciences, often with certifications in clinical trials
Work EnvironmentResearch labs, pharmaceutical companies, biotech firmsClinical trial sites, hospitals, research organizations
Employer & Industry UsagePharmaceutical, biotech, medical device companiesContract research organizations, pharmaceutical companies
Common Search & ComparisonYesYes

The Associate Clinical Scientist and Clinical Research Associate roles share similarities in industry and required credentials, but differ mainly in work environment and focus. The Associate Clinical Scientist typically works in research labs or biotech firms focusing on data analysis and scientific development, while the Clinical Research Associate is more involved in monitoring clinical trials at trial sites. Both roles are essential in the clinical research process, with overlapping skills and industry usage.

What are the most commonly searched types of Clinical Scientist jobs in Michigan?

The most popular types of Clinical Scientist jobs in Michigan are:

What are popular job titles related to Associate Clinical Scientist jobs in Michigan?

For Associate Clinical Scientist jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Associate Clinical Scientist jobs in Michigan look for?

The top searched job categories for Associate Clinical Scientist jobs in Michigan are:

What cities in Michigan are hiring for Associate Clinical Scientist jobs?

Cities in Michigan with the most Associate Clinical Scientist job openings:

Associate Clinical Scientist jobs near you
Infographic showing various Associate Clinical Scientist job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 27% Part Time, 3% Temporary, 2% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $99,255 per year, or $47.7 per hour.

Research Associate, Clinical/Population Sciences - Office of Women's Health

Wayne State University

Detroit, MI • On-site

Full-time

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

Wayne State University rating

7.6

Company rating: 7.6 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

289th of 621 rated colleges and universities

Job description

Research Associate, Clinical/Population Sciences - Office of Women's Health
Wayne State University is searching for an experienced Research Associate, Clinical/Population Sciences - Office of Women's Health 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):
Under the direction of the Principal Investigator, provide scientific, technical, regulatory, and administrative assistance to support clinical research studies. Assist in the development of research projects related to women's health through literature review, data collection and analysis, and the other research activities, as appropriate. Contribute to the dissemination of research findings, support trainee mentorship, and participate in collaborative, educational, and community engagement activities.
Support the design and implementation of clinical research protocols involving human subjects. Conduct literature reviews to identify current knowledge gaps and emerging research trends related to the Project of Interest. Communicate regularly with the Principal Investigator and research team regarding study progress.
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. Write scientific manuscripts and other documents for publication. Draft, fact-check, edit, and proofread scientific manuscripts, study reports, and regulatory documents.
Mentor students and volunteers, contribute to the design of their research projects, and provide scientific guidance throughout project implementation and completion. Participate and organize community engagement programs.
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.
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:
Qualifications:
Education: Master's degree
  • Bachelor's degree from an accredited college or university in in a field of science or learning.

  • Doctorate preferred.

Experience: Intermediate (3 to 4 years job-related experience)
  • Experience conducting clinical or human subjects research is preferred.

  • Experience in research activities, including literature review, experimental protocol design, data analysis, and interpretation of research findings.

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), Canva 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:
School/College/Division:
H39 - VP for Health Affairs
Primary department:
H3902 - Women's Health
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 local travel for 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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