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≈ $63k – $174k per year (Estimated)
Location
In office (Dallas)

Confirmed on the employer's own hiring board on Sep 25, 2026. First seen by Alion on Sep 24, 2026.

Overview
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Impact
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We are developing blood tests that detect cancer in its earliest stages so we can transform cancer into a disease that’s preventable and curable.

About our Company: 

Universal DX, Inc.is an internationalCompanywith a highly experienced team focused on cracking cancer’s code. Through our multi-omics and bioinformatics models, we have figured out how to read the disease’s signals in blood with high accuracy to detect cancerin its earliest stages. Starting with a colorectal cancerscreeningliquid biopsy test, we are building a multi-cancer platform that can identifythe unique DNA regions associated with different typesof cancers. 

The Opportunity:  

Universal DX is seeking an R&D Research Associate to support the continued development and refinement of Signal-C, our next-generation sequencing (NGS) assay for colorectal cancer screening. You will execute customized study protocols with training and guidance from scientists, help investigate unexpected results, and contribute to improvements in assay chemistry and performance. 

This hands-on, onsite role in Dallas Fort Worth calls for a foundation in molecular biology and the ability to learn new methods and carry out study-specific protocols. You will work across plasma cfDNA extraction, library preparation, target capture, and sequencing using manual and automated methods. 

 You will be part of a team that is passionate about developing novel diagnostic tests for the early detection of cancers. As part of the team, you will be in a Company that aims more than to become one of the leaders in the industry. We want to have a huge positive impact on society by achieving the ambitious purpose of “making cancer a curable disease by detecting it earlier”. 

How you’ll contribute:  

  • Help scientists prepare bench protocols and run plans. Execute bespoke studies with guidance as needed, documenting experimental variables, controls, and protocol revisions. 
  • Process plasma and extract cell-free DNA (cfDNA); perform library preparation, methylation conversion, PCR, bead cleanup, target capture, and sequencing. Support whole-blood processing when required by a study. 
  • Set up and run Hamilton or similar liquid handlers after training; verify deck layouts, worklists, labware, and study-specific parameters, and raise method or run issues with Automation. 
  • Prepare reagent mixes, dilutions, controls, plate maps, and library pools; check calculations, sample availability, identities, index assignments, and sequencing sample sheets. 
  • Assess DNA and library yield, purity, and size using TapeStation and other quantification methods. Review QC results and flag variability for follow-up with scientists. 
  • Support optimization, robustness, stability, and verification studies evaluating extraction conditions, library chemistry and adapters, capture panels, and processing parameters. 
  • Assist in investigating unexpected results by checking controls, sample quality, reagents, reaction conditions, and automation performance; document observations and carry out follow-up experiments with scientists. 
  • Maintain complete experiment and LIMS records covering protocol changes, results, deviations and corrective actions, reagent lots, instrument settings, sample IDs, remaining volumes, and storage/freeze-thaw history. 
  • Summarize results for review; support protocols, SOPs, reports, and training materials. Coordinate with scientists, Molecular Technologists, Automation, Bioinformatics, Quality, and sample-management colleagues. 
  • Perform and document routine equipment checks and maintenance. Follow safety and contamination-control procedures for human specimens, chemicals, and hazardous waste. 

What you’ll bring:  

Required Qualifications  

  • Bachelor’s degree in molecular biology, biochemistry, genetics, biotechnology, biomedical or biomechanical engineering, or a related field. 
  • Hands-on molecular biology experience through academic research, internships, or industry laboratory work, including DNA extraction, quantification and purification, PCR, reagent preparation, and accurate dilution calculations. 
  • Familiarity with automated liquid handlers or comparable laboratory automation, and ability to learn Hamilton run setup, monitoring, and basic troubleshooting. 
  • Ability to follow multistep protocols and learn study-specific variations with guidance, with a basic understanding of molecular biology principles, experimental controls, and sources of variability. 
  • Ability to recognize unexpected results, review quantitative data, and assist with troubleshooting, seeking guidance from scientists or Automation when needed. 
  • Working knowledge of Microsoft Excel and Word or equivalent tools for reagent calculations, basic data summaries, plots, and clear laboratory documentation. 
  • Strong organizational skills and attention to detail; ability to organize assigned experiments, protect limited sample material, and communicate findings and issues clearly. 
  • Ability to work onsite in Dallas Fort Worth, maintain traceable experimental records, and follow laboratory quality, human-specimen safety, and contamination-control procedures. 

Preferred Qualifications  

  • Master’s degree in molecular biology, biochemistry, genetics, biotechnology, biomedical or biomechanical engineering, or a related field. 
  • Hands-on NGS experience, including library preparation, hybridization-based target capture, library pooling, and sequencing on Illumina platforms. 
  • Familiarity with cfDNA methylation sequencing, including enzymatic methylation conversion, and experience handling low-input cfDNA or liquid biopsy samples. 
  • Experience running Hamilton liquid-handling methods, performing routine instrument checks, and troubleshooting automated runs. 
  • Experience with TapeStation or comparable fragment-analysis instruments and fluorometric or qPCR-based DNA/library quantification. 
  • Experience in assay development or optimization, including evaluating new reagents or protocols and supporting robustness, stability, or verification studies. 
  • Familiarity with LIMS, electronic notebooks, and IVD development or CLIA/CAP laboratory documentation, including SOPs, deviations, corrective actions, and sample traceability. 

What we'll offer:  

We’re proud to offer exceptional corporate benefits which include: 

  • 22 days of PTO with the possibility to carry over 10 days to the following year. 
  • Company Holidays, plus your Birthday off!  
  • Company-sponsored benefit plans, including medical, dental, and vision insurance plus life, STD, and LTD coverage, and 401(k). 
  • Flexible work schedule  
  • And more to come! 

  Why Now?  

This is an exciting time to be at Universal DX. We are growing rapidly and starting our US operations by building up our team, starting our lab and business operations, and establishing strategic partnerships.  

We are looking for passionate changemakers to be a part of our journey in this expansive time for us. 

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