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Single Cell Rna Sequencing Jobs in Delaware (NOW HIRING)

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Single Cell Rna Sequencing information

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$12

$21

$30

How much do single cell rna sequencing jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for single cell rna sequencing in Delaware is $21.66, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $27.16 per hour, depending on experience, location, and employer.

What is single cell RNA sequencing?

Single cell RNA sequencing (scRNA-seq) is a technique that allows researchers to examine the gene expression profiles of individual cells. Unlike traditional RNA sequencing, which measures average gene expression across thousands or millions of cells, scRNA-seq reveals the unique transcriptomic signature of each cell. This method is valuable for studying cellular diversity, identifying rare cell types, and understanding complex biological processes such as development, disease progression, and immune responses.

What are the key skills and qualifications needed to thrive as a single cell RNA sequencing specialist?

To thrive as a Single Cell RNA Sequencing Specialist, you need a solid background in molecular biology, genomics, and data analysis, typically supported by a relevant degree in the life sciences. Familiarity with sequencing platforms (such as 10x Genomics or Illumina), bioinformatics tools (like Seurat or Cell Ranger), and experience with data visualization are crucial. Attention to detail, problem-solving ability, and strong communication skills help ensure accurate results and effective collaboration with research teams. Mastering these skills is essential for generating high-quality data, troubleshooting experiments, and translating complex findings into actionable insights.

What are some common challenges faced by researchers working in single cell RNA sequencing, and how can they be addressed?

Researchers in Single Cell RNA Sequencing often encounter challenges such as sample preparation variability, data complexity, and managing large datasets. Ensuring high-quality single-cell suspensions and minimizing cell loss during processing are critical steps. Additionally, interpreting data requires proficiency with bioinformatics tools and collaboration with computational biologists. Staying up-to-date with evolving protocols and leveraging multi-disciplinary teamwork can help address these challenges effectively.

What is the difference between Single Cell Rna Sequencing vs Single Cell Genomics Technician?

AspectSingle Cell Rna SequencingSingle Cell Genomics Technician
CredentialsTypically requires a degree in biology, molecular biology, or related fields; experience with sequencing technologiesSimilar credentials; often with laboratory or technical certifications in genomics
Work EnvironmentLaboratories performing sequencing, data analysis, and sample preparationLaboratories focused on sample processing, sequencing support, and data collection
Industry UsageUsed in research labs, biotech, and pharmaceutical companies for gene expression studiesCommon in genomics research centers, biotech firms, and academic labs

Both roles involve working with genomic technologies and require similar educational backgrounds. However, Single Cell Rna Sequencing specialists focus more on RNA analysis and data interpretation, while Single Cell Genomics Technicians support sample preparation and sequencing workflows. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Single Cell Rna Sequencing jobs in Delaware?

For Single Cell Rna Sequencing jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Single Cell Rna Sequencing jobs in Delaware look for?

The top searched job categories for Single Cell Rna Sequencing jobs in Delaware are:

What cities in Delaware are hiring for Single Cell Rna Sequencing jobs?

Cities in Delaware with the most Single Cell Rna Sequencing job openings:

Single Cell Rna Sequencing jobs near you

Scientific Director, Research

Nemours Children's Health

Wilmington, DE • On-site

Full-time

Posted 14 days ago

Nemours Children's Health rating

8.1

Company rating: 8.1 out of 10

Based on 87 frontline employees who took The Breakroom Quiz

66th of 898 rated healthcare providers

Job description


Nemours Children's Health is seeking an innovative and collaborative PhD-level Research Scientist to join the Biobank and Molecular Analysis Program (BMAP) and serve as Scientific Director.
This position will provide scientific leadership and consultation to investigators across Nemours and collaborating institutions by supporting study development, experimental design, grant applications, molecular assay development, and translational research initiatives.
The successful candidate will serve as a key scientific partner to principal investigators, clinicians, physician-scientists, and research teams, helping transform research questions into rigorous, fundable, and executable projects. The position will leverage the extensive capabilities of BMAP, including biobanking, molecular biology, genomics, next-generation sequencing, spatial transcriptomics, and DNA methylation technologies to support cutting-edge pediatric research and precision medicine initiatives.
In addition, this individual will function as the Technical Supervisor for the Nemours Genomics Laboratory (NGL), overseeing implementation, validation, quality management, and regulatory compliance for current and future next-generation sequencing assays and other molecular diagnostic tests.
This position offers a unique opportunity to build and expand an integrated pediatric genomics and translational research program within a nationally recognized children's health system. The successful candidate will work alongside investigators across multiple specialties while helping shape the future of precision medicine, molecular diagnostics, and pediatric genomics at Nemours Children's Health.
Primary Responsibilities
Scientific Collaboration and Research Development
  • Partner with principal investigators, clinicians, and research teams throughout Nemours (pathology, oncology, genomics, bioinformatics, and translational science teams) to develop multidisciplinary collaborations and innovative research programs utilizing BMAP core resources.
  • Provide expert consultation on experimental design, study feasibility, sample requirements, statistical considerations, technology selection, and biomarker development on initiative of importance to the program.
  • Assist investigators with development of grant applications, preliminary data generation, scientific manuscripts, and collaborative research proposals for investigators utilizing the program.
  • Identify emerging molecular technologies and incorporate them into BMAP program.
  • Support investigators in utilizing BMAP resources to maximize scientific productivity and successful funding outcomes.

Genomics and Molecular Biology Leadership
Provide expertise in:
  • DNA and RNA based next generation sequencing (Illumina platform)
  • Targeted sequencing panels
  • Whole exome and transcriptome applications
  • Single-cell genomics technologies (10x Genomics)
  • Spatial transcriptomics and spatial biology applications (10x Genomics)
  • DNA methylation profiling and epigenetic studies
  • Gene expression analysis
  • Digital PCR
  • Genotyping and SNP analysis
  • Cell line authentication
  • Biomarker discovery and validation
  • Clinical and translational genomics

Technical Supervisor, Nemours Genomics Laboratory
  • Serve as Technical Supervisor for CAP/CLIA-regulated molecular diagnostic testing.
  • Lead development, validation, verification, and implementation of molecular diagnostic assays.
  • Support launch and ongoing oversight of NGS-based clinical testing within the Nemours Genomics Laboratory.
  • Develop and maintain laboratory procedures, quality systems, and validation plans.
  • Ensure compliance with CAP, CLIA, and applicable regulatory requirements.
  • Participate in proficiency testing, quality assurance, quality management, and inspection readiness activities.
  • Provide technical oversight for troubleshooting, assay optimization, and workflow improvements.
  • Work closely with laboratory leadership, pathologists, technologists, and bioinformatics personnel to expand the test menu.

Biobank and Translational Research Infrastructure
  • Provide oversight of BMAP CAP-accredited pediatric biorepository including QMS program, re-accreditation processes, and applicable regulatory requirements.
  • Provide oversight of all biospecimen processing and storage processes.
  • Develop and maintain all laboratory processes and procedures at a level of CAP accreditation requirements.
  • Participate in competency testing, quality assurance, quality management and inspection readiness activities.

Required Qualifications
  • Master Degree required, PhD in Molecular Biology, Genetics, Genomics, Cancer Biology, Biomedical Sciences, Molecular Pathology, or related discipline strongly preferred
  • Minimum 5 years of postdoctoral, academic, industry, or translational research experience.
  • Demonstrated expertise in molecular biology and genomics technologies.
  • Experience designing and leading collaborative research projects.
  • Experience with next-generation sequencing workflows and assay development.
  • Strong scientific publication and grant support record.
  • Excellent communication and interdisciplinary collaboration skills.
  • Demonstrated ability to mentor investigators, trainees, and laboratory personnel.

Preferred Qualifications
  • Experience serving in a technical leadership or supervisory role within a molecular laboratory.
  • Knowledge of CAP, CLIA, and molecular diagnostic regulatory requirements.
  • Experience with laboratory test validation and quality management programs.
  • Experience with spatial transcriptomics and spatial biology technologies.
  • Experience with DNA methylation arrays and epigenetic analysis.
  • Familiarity with pediatric oncology, rare diseases, precision medicine, or translational research.
  • Experience working in a CAP and/or CLIA regulated environment.
  • Familiarity with bioinformatics pipelines and genomic data interpretation.

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About Us
Nemours Children's Health is an internationally recognized pediatric health system serving more than 1.7 million patient encounters each year. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
Backed by the Nemours Foundation and Alfred I. duPont Trust, our $1.7B nonprofit system is dedicated to improving children's health through clinical care, research, education, advocacy, and prevention. Our Whole Child Health approach focuses equally on prevention and treatment, partnering with communities to help every child thrive.
Inclusion and belonging guide our strategy and growth. We are committed to culturally relevant care, reducing health disparities, and fostering an environment where every associate, patient, and family feels supported and valued.
Learn more at Nemours.org.

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About Nemours

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As one of the nation's leading pediatric health care systems, Nemours is committed to providing all children with their best chance to grow up healthy. We offer integrated, family-centered care to more than 300,000 children each year in our pediatric hospitals, specialty clinics, primary care practices, and school-based health centers in Delaware, Florida, Maryland, New Jersey and Pennsylvania. Nemours strives to ensure a healthier tomorrow for all children - even those who may never enter our doors - through our world-changing research, education and advocacy efforts.

Industry

Health care and social assistance and hospitals

Company size

1,001 - 5,000 Employees

Headquarters location

Jacksonville, FL, US

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