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Entry Level Clinical Genomic Scientist Jobs (NOW HIRING)

Belay Diagnostics

Clinical Data Abstractor

Chicago, IL · On-site

The Clinical Data Abstractor will work closely with Clinical Genomic Analysts/Scientists and laboratory personnel to promote accurate, efficient, and timely patient reporting.Must be eligible to work ...

Mayo Clinic

Clinical Geneticist

Rochester, MN

$208K - $708K/yr

The Department of Clinical Genomics partners with several centers within Mayo Clinic, including the Center for the Science of Health Care Delivery, the Center for Regenerative Medicine, the Center ...

Mayo Clinic

Clinical Geneticist

Rochester, MN · On-site

The Department of Clinical Genomics partners with several centers within Mayo Clinic, including the Center for the Science of Health Care Delivery, the Center for Regenerative Medicine, the Center ...

Mayo Clinic

Clinical Geneticist

Rochester, MN

The Department of Clinical Genomics partners with several centers within Mayo Clinic, including the Center for the Science of Health Care Delivery, the Center for Regenerative Medicine, the Center ...

Mayo Clinic

Clinical Geneticist

Rochester, MN · On-site

The Department of Clinical Genomics partners with several centers within Mayo Clinic, including the Center for the Science of Health Care Delivery, the Center for Regenerative Medicine, the Center ...

Nationwide Children's Hospital

Provides scientific assessment for evaluation and implementation of relevant, state of the art clinical cytogenetic, molecular genetic, and genomic services, including the interpretative analysis of ...

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Entry Level Clinical Genomic Scientist information

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How much do entry level clinical genomic scientist jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for entry level clinical genomic scientist in the United States is $54.75, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $68.27 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Clinical Genomic Scientist vs Entry Level Molecular Laboratory Technician?

AspectEntry Level Clinical Genomic ScientistEntry Level Molecular Laboratory Technician
CredentialsBachelor's degree in genetics, biology, or related field; certification preferredBachelor's degree in biology, chemistry, or related field; certification often not required
Work EnvironmentClinical laboratories, hospitals, research institutionsResearch labs, diagnostic labs, hospitals
Employer & IndustryHealthcare, diagnostics, biotech companiesResearch institutions, diagnostic labs, biotech firms
Common Search & ComparisonYesYes

The Entry Level Clinical Genomic Scientist typically requires specialized knowledge in genomics and often certification, working mainly in clinical settings. In contrast, the Entry Level Molecular Laboratory Technician focuses on laboratory procedures with less emphasis on genomics-specific training. Both roles are essential in healthcare and research, but the genomic scientist role involves more advanced interpretation of genetic data.

What are the key skills and qualifications needed to thrive as an entry level clinical genomic scientist?

To thrive as an Entry Level Clinical Genomic Scientist, you need a solid background in genetics, molecular biology, and bioinformatics, typically supported by a bachelor’s or master’s degree in a relevant field. Familiarity with next-generation sequencing (NGS) platforms, data analysis software, and laboratory information management systems (LIMS) is commonly required. Attention to detail, problem-solving abilities, and strong communication skills help ensure accuracy and effective collaboration with clinical teams. These competencies are vital for delivering reliable genomic data and supporting accurate clinical decision-making in healthcare settings.

What does an entry level clinical genomic scientist do?

As an entry level clinical genomic scientist, you will typically assist with genomic data analysis, variant interpretation, and laboratory workflows under the supervision of senior scientists. Your responsibilities may include preparing samples, conducting quality control checks, and helping interpret genetic test results for clinical reports. You’ll often collaborate with laboratory technologists, genetic counselors, and clinicians to ensure accurate and timely data delivery. The first year is focused on building your technical skills and understanding clinical genomics guidelines, which sets a strong foundation for more independent work as you gain experience.

What is an entry level clinical genomic scientist?

Entry level clinical genomic scientists are professionals who analyze genetic data to assist in the diagnosis and management of diseases. They typically work in clinical laboratories, hospitals, or research institutions under the supervision of experienced scientists. Their responsibilities include performing genetic tests, interpreting results, maintaining laboratory equipment, and ensuring quality control. This role often serves as a starting point for those who have recently completed a degree in genetics, biology, or a related field and are seeking to gain hands-on experience in clinical genomics.
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Entry Level Clinical Genomic Scientist jobs near you
Infographic showing various Entry Level Clinical Genomic Scientist job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $113,877 per year, or $54.7 per hour.

Clinical Data Abstractor

Belay Diagnostics

Chicago, IL

Full-time

Posted 5 days ago

Job description

Under general supervision of the Director of Laboratory Operations and in collaboration with the Analysis and Reporting team, the Clinical Data Abstractor will support the clinical laboratory by reviewing patient medical records, organizing clinical information, and preparing cases for downstream analysis including post-accessioning second review. This position is responsible for abstracting key clinical data from electronic health records, preparing standardized case documentation, maintaining laboratory databases, ensuring required documentation is complete, and supporting laboratory workflows through administrative and operational activities. The Clinical Data Abstractor will work closely with Clinical Genomic Analysts/Scientists and laboratory personnel to promote accurate, efficient, and timely patient reporting.Must be eligible to work in the United States.


Responsibilities:

  • Review patient medical records, pathology reports, and laboratory results to identify, abstract, and organize clinically relevant information
  • Perform quality review of incoming samples by reviewing test requisition forms (TRFs), specimen labels, patient demographics, and supporting documentation. Collaborate with the Customer Service team to resolve discrepancies, obtain missing documentation, and ensure cases meet laboratory requirements prior to analysis
  • Prepare clinical summaries and case documentation by organizing patient demographics, clinical history, previous genomic testing and findings, and test order information to support variant interpretation and clinical reporting
  • Maintain internal laboratory databases, spreadsheets, knowledge resources, and other records that support clinical reporting and laboratory operations
  • Provide administrative and operational support for laboratory workflows, quality improvement initiatives, documentation, and other projects that support the clinical laboratory
  • Performs general duties such as maintaining safety records in adherence to compliance in line with established protocols
  • Maintains effective communication within the department and with other internal and external clinical and research professionals
  • Maintain a positive attitude when faced with challenges


Education and Experience Qualifications:

  • Bachelor's degree in Biology, Genetics, Molecular Biology, Biomedical Sciences, Health Sciences, Nursing, Public Health, or a related scientific discipline
  • Prior experience in regulated laboratory environment (e.g. CLIA, CAP) is preferred


Required knowledge:

  • Familiarity with specimen receipt, review of TRFs, and accessioning workflows
  • Understanding of medical/oncology terminology, pathology reports, and/or genomic testing is preferred
  • Strong organizational skills and attention to detail
  • Excellent written and verbal communications skills
  • Work successfully in a multidisciplinary team environment
  • Ability to manage multiple priorities while maintaining a high level of accuracy

Apply