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Clinical Research Associate Bridge Program Jobs in Michigan

Clinical Research Coordinator

Detroit, MI · On-site

$24 - $31.75/hr

Clinical Research Coordinator This role focuses on coordinating complex clinical drug trials within ... Benefits are subject to change and may be subject to specific elections, plan, or program terms. If ...

Clinical Research Coordinator

Detroit, MI · On-site

$24 - $31.75/hr

Clinical Research Coordinator This role focuses on coordinating complex clinical drug trials within ... Benefits are subject to change and may be subject to specific elections, plan, or program terms. If ...

Clinical Research Coordinator

Detroit, MI

$24 - $31.75/hr

Clinical Research Coordinator This role focuses on coordinating complex clinical drug trials within ... Benefits are subject to change and may be subject to specific elections, plan, or program terms. If ...

Clinical Research Nurse This role provides specialized nursing care to participants enrolled in ... Benefits are subject to change and may be subject to specific elections, plan, or program terms. If ...

New

Clinical Research Coordinator-Hematology

Detroit, MI · On-site

$24 - $31.75/hr

Interest in ongoing professional development, including participation in internal training programs ... clinical research setting. The coordinator typically starts between 7:00 a.m. and 9:00 a.m ...

Clinical Research Coordinator This role focuses on coordinating complex clinical drug trials within ... Benefits are subject to change and may be subject to specific elections, plan, or program terms. If ...

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Clinical Research Associate Bridge Program information

See Michigan salary details

$10

$35

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How much do clinical research associate bridge program jobs pay per hour?

As of Jun 27, 2026, the average hourly pay for clinical research associate bridge program in Michigan is $35.85, according to ZipRecruiter salary data. Most workers in this role earn between $25.14 and $45.87 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate in a bridge program, and why are they important?

To thrive as a Clinical Research Associate in a bridge program, you need a foundational understanding of clinical trials, regulatory compliance, and data management, usually supported by a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, effective communication, and organizational skills help you manage study protocols and collaborate with diverse teams. These competencies are crucial for ensuring clinical trial integrity, regulatory adherence, and the successful execution of research studies.

What types of mentorship and training can I expect as a participant in a Clinical Research Associate Bridge Program?

Participants in a Clinical Research Associate (CRA) Bridge Program typically receive structured mentorship from experienced CRAs and clinical research professionals. The program often includes hands-on training in protocol review, site monitoring, regulatory compliance, and data management, combined with classroom or online learning modules. You'll work closely with cross-functional teams, such as clinical project managers and regulatory specialists, gaining exposure to industry-standard processes and tools. This supportive environment is designed to accelerate your transition into a CRA role and help you build a strong professional network within clinical research.

What is a Clinical Research Associate Bridge Program?

A Clinical Research Associate (CRA) Bridge Program is a specialized training course designed to help individuals transition into the role of a CRA, especially those with related experience in healthcare, life sciences, or clinical research support. These programs typically combine classroom instruction with practical training, focusing on topics such as clinical trial monitoring, regulatory compliance, and Good Clinical Practice (GCP) guidelines. The goal is to equip participants with the necessary knowledge and skills to begin a career as a CRA, often including job placement assistance or internships. Bridge programs are ideal for those who want to move into clinical research from a related field but lack direct CRA experience.
What are popular job titles related to Clinical Research Associate Bridge Program jobs in Michigan? For Clinical Research Associate Bridge Program jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Clinical Research Associate Bridge Program jobs in Michigan look for? The top searched job categories for Clinical Research Associate Bridge Program jobs in Michigan are:
What cities in Michigan are hiring for Clinical Research Associate Bridge Program jobs? Cities in Michigan with the most Clinical Research Associate Bridge Program job openings:
Research Associate - Department of Oncology

Research Associate - Department of Oncology

Wayne State University

Detroit, MI • On-site

Full-time

Posted 26 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

246th of 541 rated colleges and universities


Job description

Research Associate - Department of Oncology
Wayne State University is searching for an experienced Research Associate - 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):
Perform laboratory based scientific techniques or clinical/population science (human subjects) research. Design and perform experiments, recruit participants for studies by developing surveys and interviewing candidates. Participate in implementing research objectives, ensuring compliance with all legal, regulatory and protocol guidelines. Assist staff with experiments /research protocols as required. Communicate with principal investigator and Postdoctoral scholars/fellows on the status of research.
Collect and log laboratory results, clinical outcomes and/or survey data. Evaluate and perform data analysis using graphs, charts or tables to highlight the key points of the research results collected in accordance with the research protocols as stipulated. Proofread and edit research data and documents to ensure accuracy.
Prepare and present presentations regarding research results for professional, scientific and academic conferences. Summarize and organize data results for submittal to academic and scholarly, peer-reviewed journals. Write scientific manuscripts and other documents for publication. Fact-check, proofread, and edit research documents to ensure accuracy.
Maintain the laboratory work areas including routine maintenance on laboratory equipment as required. Order and organize required research supplies and records. Maintain cleanliness and organization of work station.
Perform other related duties as assigned.
Unique duties:
Maintain tissue-processing and histology infrastructure required for cancer clinical research, ensuring continuity, quality, and regulatory-aligned performance of biospecimen services. - Perform routine and specialized staining (including H&E), immunohistochemistry (IHC), and immunofluorescence (IF), and participates in antibody optimization and validation. - Monitor pre-analytical variables, maintains detailed documentation in accordance with biobanking SOPs and CAP/CLIA-aligned research standards, and supports digital pathology workflows, including whole-slide imaging, digital annotation, and quantitative image analysis.
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: Experienced (minimum 2 years of job-related experience)
Experience performing basic research techniques, preferred.
Knowledge, Skills and Abilities:
Ability to work independently. Ability to analyze, summarize and interpret research findings in reports and communicate results. Knowledge of scientific integrity principles. Excellent time management and organization skills. Excellent interpersonal skills and demonstrated ability to work with others in a collaborative environment. Microsoft office software skills.
Preferred qualifications:
- Experience with human tissue histology, including FFPE and frozen sectioning. - Proficiency in H&E staining and immunohistochemistry. - Strong attention to detail and commitment to quality and reproducibility. - Experience working in a cancer center, biobank, or translational research core. - Familiarity with multiplex IHC/IF, spatial biology platforms, or laser capture microdissection. - Experience with digital pathology systems and image analysis software.
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
  • Hourly rate:
  • Salary minimum:
  • Salary hire maximum:
Working conditions:
Typical work environment may include a laboratory and/ or office environment. May require working non-standard business hours including 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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