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Clinical Research Trainee Jobs in Renton, WA (NOW HIRING)

EEG Tech Trainee

Tacoma, WA · On-site

$29.12/hr

Whether you're looking to advance your research, take on leadership opportunities, or be part of ... Robust support Clinical, administrative and IT resources that allow you to focus on patient care ...

DEPARTMENT DESCRIPTION Advanced diagnostic imaging, specialized clinical expertise. Radiology ... Nearly 29,000 healthcare professionals, researchers, and educators work in the UW Medicine family ...

Staff Scientist

Seattle, WA · On-site

$72K - $111K/yr

... clinical samples and translational research studies. * Familiarity with computational analysis tools and collaboration with bioinformatics teams. * Prior experience mentoring trainees and ...

Showing results 41-60

Clinical Research Trainee information

What is a clinical research trainee?

Clinical Research Trainees are individuals, often students or recent graduates, who are gaining practical experience in the field of clinical research. They assist in the design, implementation, and monitoring of clinical trials under the supervision of experienced researchers. Their responsibilities may include data collection, managing study documentation, ensuring compliance with regulatory guidelines, and supporting patient recruitment. The role provides foundational knowledge and hands-on skills necessary for a career in clinical research or related healthcare fields.

What are the key skills and qualifications needed to thrive as a clinical research trainee, and why are they important?

To thrive as a Clinical Research Trainee, you need a solid background in life sciences or healthcare, attention to detail, and a foundational understanding of research methodologies, typically supported by a relevant degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and clinical trial management software is essential. Strong organizational skills, effective communication, and the ability to collaborate within multidisciplinary teams are standout soft skills. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What are the typical responsibilities of a clinical research trainee during a clinical trial?

As a Clinical Research Trainee, you will typically assist with the coordination and execution of clinical trials under the supervision of experienced research staff. Your daily tasks may include collecting and managing patient data, assisting with patient recruitment and informed consent, preparing study documentation, and ensuring compliance with regulatory guidelines. Trainees often collaborate closely with clinical teams, principal investigators, and external partners, gaining hands-on experience across various study phases. This role provides valuable exposure to clinical research protocols and is a great foundation for advancing into more senior research or coordinator positions.

What is the difference between Clinical Research Trainee vs Clinical Research Coordinator?

AspectClinical Research TraineeClinical Research Coordinator
Required CredentialsTypically pursuing or holding a relevant degree (e.g., life sciences, healthcare)Usually has a degree or certification in clinical research or related field
Work EnvironmentTraining setting, often in academic or research institutionsActive role in managing clinical trials at research sites or hospitals
Employer & Industry UsageEducational programs, research institutions, pharmaceutical companiesHospitals, clinics, research organizations
Common Search & Comparison IntentUnderstanding entry-level roles and training opportunitiesClarifying responsibilities and career progression in clinical research

While both roles are involved in clinical research, a Clinical Research Trainee is typically in a learning or internship phase, gaining foundational knowledge. In contrast, a Clinical Research Coordinator actively manages and oversees clinical trials, requiring more experience and responsibility.

What are the most commonly searched types of Clinical Research jobs in Renton, WA? The most popular types of Clinical Research jobs in Renton, WA are:
What are popular job titles related to Clinical Research Trainee jobs in Renton, WA? For Clinical Research Trainee jobs in Renton, WA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Trainee jobs in Renton, WA look for? The top searched job categories for Clinical Research Trainee jobs in Renton, WA are:
What cities near Renton, WA are hiring for Clinical Research Trainee jobs? Cities near Renton, WA with the most Clinical Research Trainee job openings:
Infographic showing various Clinical Research Trainee job openings in Renton, WA as of July 2026, with employment types broken down into 100% Full Time. Highlights an 49% In-person, and 51% Remote job distribution.

Research Scientist/Engineer 3

University of Washington

Seattle, WA • On-site

Full-time

Re-posted 11 days ago


University Of Washington School Of Medicine rating

8.0

Company rating: 8.0 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

187th of 618 rated colleges and universities


Job description

Job Description
The Division of Metabolism, Endocrinology and Nutrition (MET) has an outstanding opportunity for a Research Scientist/Engineer 3 position to support studies within the Pyle and Bjornstad Laboratories.
Housed within the University of Washington Medicine Diabetes Institute at the South Lake Union campus, the Pyle laboratory applies translational data science to bridge complex biostatistics and bioinformatics findings into medical insights. The Bjornstad and Pyle laboratories focus on metabolic and hemodynamic mechanisms underlying the development of diabetic kidney disease (DKD) and cardiovascular disease (CVD) in Type 1 (T1D) and Type 2 (T2D) diabetes and obesity.
This position is engaged in the field of Spatial transcriptomics and bioinformatics. This position supports the analysis of spatial transcriptomic data generated from kidney biopsy tissue using 10x Genomics platforms including Visium, Visium HD, and Xenium Prime 5K. The role involves processing, quality control, and interpretation of spatially resolved gene expression data to understand disease mechanisms in diabetic kidney disease and obesity-related kidney disease. A key focus includes cell type deconvolution, integration with single-cell RNA-seq reference data, identification of spatially variable genes, and pathway enrichment analysis. This position requires effective communication of results through manuscript writing and presentations at conferences. This position will work under general guidance, receiving instruction on specific assignment objectives, and will collaborate with investigators on spatial transcriptomic analyses, data visualization, and preparation of abstracts, talks, and manuscripts.
Research Sponsors/Stakeholders: Novo Nordisk and NIH
DUTIES AND RESPONSIBILITIES
Spatial Transcriptomics and Data Analysis 60%
• Process and quality-control 10x Genomics Visium, Visium HD, and Xenium Prime 5K spatial transcriptomics data from human and mouse kidney tissue
• Perform spatial preprocessing with Space Ranger and downstream integration across samples using Seurat and BPCells
• Perform cell type deconvolution and mapping by integrating spatial data with single-cell RNA-seq reference objects using RCTD (spacexr) workflow
• Identify spatially variable genes and cluster-specific markers to prioritize biological pathways and candidate genes for downstream investigation
• Perform differential expression and pathway enrichment analysis using decoupleR, clusterProfiler, and GSEA
• Perform image stitching and alignment using ImageJ and Loupe Browser for spatial preprocessing
• Integrate multi-sample spatial datasets to enable scalable normalization, clustering, and cross-sample comparison
• Develop protocol-specific systems and documents including process flows, training manuals, and Standard Operating Procedures (SOPs).
• Maintain subject level documentation and prepares documents, equipment and/or supplies
• Provide the biostatistical/data science expertise and leadership in study design, study oversight, data management, data analysis and manuscript preparation to assist all levels of biomedical investigators and clinicians on new research activities across a wide range of disciplines
• Provide mentorship to collaborators, trainees, and team members
• Acts as a subject matter expert and authority in the areas of data management and data analysis
• Serve as an expert resource to PIs and other stakeholders
Bioinformatics Programming 20%
• Assist with the design and development of major bioinformatics-related programming projects
• Write custom scripts to access databases, analyze data, and create reproducible visual representations of results
• Write custom web tools for PIs and other stakeholders
Laboratory support 20%
• Collaborate on the preparation and presentation of data for publications in peer-reviewed journals, ensuring clarity and adherence to publication standards.
• Assist Team Leads, Supervisors, and management in developing and implementing effective processes, procedures, and quality improvement initiatives that enhance team performance.
• Develop and disseminate a variety of tools designed to access relevant clinical and sample data
• Provide guidance and training to junior team members, fostering a culture of continuous learning and professional development.
• Identify and analyze operational efficiency issues, communicating findings and recommendations to leadership for informed decision-making.
• Proactively identify and recommend training and development opportunities for both new hires and existing team members to enhance skill sets and performance.
• Provides input and feedback to leadership on team members' overall performance, opportunities for development, and process improvement initiatives
MINIMUM QUALIFICATIONS
  • Bachelor's degree in Bioinformatics, Computational Biology, Biostatistics, Data Science or a related field and four years of relevant experience.

Equivalent education and/or experience may substitute for minimum qualifications except when there are legal requirements, such as a license, certification, and/or registration.
ADDITIONAL REQUIREMENTS
• Advanced knowledge of basic statistical principles relevant in medical research
• Experience with spatial transcriptomics platforms (10x Genomics Visium, Visium HD, and/or Xenium)
• Ability to analyze and solve complex problems and apply quantitative analytical approaches
• Demonstrated fluency in one or more programming languages (e.g., R, Python, Perl, Java, C++) and willingness to learn new programming languages as necessary
• Familiarity with statistical analytical concepts and methods
• Ability to communicate effectively, both in writing and orally
• Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
• Outstanding customer service skills
• Demonstrated commitment and leadership ability to advance diversity and inclusion
• Knowledge of basic human anatomy, physiology medical terminology
• Ability to interpret and master complex research protocol information
• Ability to handle multiple projects simultaneously within rigorous timelines
• Potential to work independently with minimal supervision and in a team atmosphere
DESIRED QUALIFICATIONS
• Experience with 10x Genomics Xenium Prime 5K spatial transcriptomics platform
• Experience with single-cell RNA-seq analysis and integration with spatial data (Seurat, spacexr/RCTD)
#UWDeptMedicineJobs
Compensation, Benefits and Position Details
Pay Range Minimum:
$80,244.00 annual
Pay Range Maximum:
$132,612.00 annual
Other Compensation:
Benefits:
For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/
Shift:
First Shift (United States of America)
Temporary or Regular?
This is a regular position
FTE (Full-Time Equivalent):
100.00%
Union/Bargaining Unit:
UAW Research
About the UW
Working at the University of Washington provides a unique opportunity to change lives - on our campuses, in our state and around the world.
UW employees bring their boundless energy, creative problem-solving skills and dedication to building stronger minds and a healthier world. In return, they enjoy outstanding benefits, opportunities for professional growth and the chance to work in an environment known for its diversity, intellectual excitement, artistic pursuits and natural beauty.
Our Commitment
The University of Washington is committed to fostering an inclusive, respectful and welcoming community for all. As an equal opportunity employer, the University considers applicants for employment without regard to race, color, creed, religion, national origin, citizenship, sex, pregnancy, age, marital status, sexual orientation, gender identity or expression, genetic information, disability, or veteran status consistent with UW Executive Order No. 81.
To request disability accommodation in the application process, contact the Disability Services Office at 206-543-6450 or dso@uw.edu.
Applicants considered for this position will be required to disclose if they are the subject of any substantiated findings or current investigations related to sexual misconduct at their current employment and past employment. Disclosure is required under Washington state law.

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