Help implement architectural guardrails across both platforms to prevent generation of non-approved clinical associations (PGx) and prohibited diagnostic disease claims (Microbiome), with validation at the model/template output layer
Work with PharmD, science, and regulatory teams to understand the boundary conditions that govern permissible output and how those constraints are encoded into the system
Application Development
Contribute to building the self-service rule and literature updating workbench (internal tooling) that enables PharmD and science teams to manage clinical rules and reference literature without engineering dependency
Help develop the clinical review portal through which technical directors and pathologists validate, annotate, and sign off on AI-generated interpretations prior to report release
Support full-stack feature development spanning backend services, REST API endpoints, and responsive front-end interfaces with a focus on clinical clarity and workflow efficiency
Learn and apply healthcare-grade security requirements: PHI data handling, encryption at rest and in transit, role-based access control, and audit logging
Assist QA/validation engineers with testing output pathways, including guardrail fuzzing and concordance testing against reference clinical interpretations
Minimum Qualifications
Current enrollment in a Bachelor's or Graduate degree program in Computer Science, Software Engineering, Data Science, Biomedical Engineering, or Bioinformatics
Preferred Qualifications
1-month plus work or coursework at a genomics laboratory, precision medicine company, diagnostics startup, or digital health platform
1-month plus familiarity with Python and/or Node.js for backend development
1-month plus experience with data pipeline or workflow orchestration tools (e.g., Airflow, Prefect, or equivalent)
1-month plus familiarity with clinical report generation standards or structured clinical language (e.g., HL7 FHIR, SNOMED CT, or RxNorm terminology)
1-month plus coursework or projects in bioinformatics, NLP, machine learning, or full-stack web development
1-month plus familiarity with cloud platforms (AWS or Azure) and containerized environments (Docker)
1-month plus front-end development experience or coursework (React, Vue, or equivalent)
1-month plus exposure to RESTful API design or web application development
Additional Job Standards
Interest in NLP, text generation, or working with large language models
Interest in genomics, molecular diagnostics, bioinformatics, pharmacogenomics, or clinical laboratory data
Strong communication skills; both written and verbal
Show initiative and the ability to work independently under general supervision
Eagerness to learn how software engineering works inside a regulated life sciences environment where patient safety and accuracy are non-negotiable
Exposure to pharmacogenomics data flows: star-allele notation, CPIC guideline structures, PharmVar reference databases, or FDA pharmacogenomic drug labeling frameworks
Exposure to microbiome sequencing data contexts (16S rRNA or metagenomic) and associated bioinformatics output formats
About the Team
Labcorp processes millions of diagnostic tests every year across genomics, molecular diagnostics, clinical chemistry, and specialty testing. Behind every test is a software stack that processes clinical data, generates interpretive reports, and delivers results to physicians and patients. This co-op role puts you inside the engineering team building that stack for two active platforms: a Pharmacogenetics (PGx) Automated Interpretive Engine and a Microbiome Clinical Context Reporting platform.
You will work across three real workstreams: helping productionize bioinformatics tooling into enterprise APIs, contributing to the NLP and language-generation layers that turn structured clinical data into physician-ready and patient-facing narratives, and building internal portals and workbenches that empower clinical and science teams to operate independently. All of this work runs under tight compliance and regulatory guardrails (HIPAA, CLIA, LDT frameworks), and you will learn firsthand how software engineering works when patient safety and regulatory accuracy are non-negotiable.
This is a rare opportunity to sit at the intersection of clinical science, responsible AI, and enterprise software engineering. You will directly contribute to how patient-level genomic and microbiome data is transformed into actionable clinical guidance, working on systems that physicians, pathologists, and patients rely on, with guardrails that matter. The work spans real engineering breadth, from API architecture and NLP pipeline design to clinical UX and regulatory compliance, making this an exceptionally high-impact co-op for a software engineer who wants their code to carry clinical and patient-level significance.
Labcorp is becoming an AI-native life sciences company. The Office of the Chief AI Officer (CAIO) leads this transformation across the entire enterprise. One of the areas the CAIO is focused on is applying AI to Labcorp's core science: how new diagnostic tests are developed, how genomic and molecular data is interpreted, how lab results are enhanced for patients and clinicians, and how AI capabilities accelerate scientific partnerships and innovation. If you want to help build the software that turns complex clinical science into real products that patients and physicians rely on, this is the role.
About the Co-op Program
As a Labcorp Co-op, you’ll be immersed in hands-on work that complements your academic background. In addition to your project work, you’ll gain valuable exposure to Labcorp’s global business through:
How production software systems are built for clinical and diagnostic use cases in a regulated healthcare environment
How NLP and language-generation pipelines transform structured clinical data (genotype calls, sequencing outputs, guideline rule sets) into physician-ready and patient-facing reports
How enterprise APIs are designed, documented, versioned, and integrated with B2B clinical and consumer platforms
How architectural guardrails enforce patient safety and regulatory compliance at the code level, not just through policy
How pharmacogenomics and microbiome data flows work, from sequencing output to interpretive report
How cross-functional collaboration works when your stakeholders are PharmDs, pathologists, regulatory teams, and clinical scientists
Co-op Details
Duration: Spring 2027 (with option for back-to-back Spring and Summer 2027)
Dates of Internship: January 2027-May 2027
Compensation: Paid Co-op
Eligibility: Preferred candidates are Sophomore, Junior standing or Graduate student who are currently enrolled in a relevant degree program; however, all current students pursuing related studies are encouraged to apply
Reports to: Executive Director, AI Architecture
Function: Full-Stack Development | NLP / Report Generation | API & Integration
This position is not eligible for visa sponsorship now or in the future.
Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please click here.
Labcorp is proud to be an Equal Opportunity Employer
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
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