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LA

Labcorp

via Workday

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Senior Scientific Program Manager - Sample to Answer Platform

Anywhere
Full-time
Posted 2/26/2026
Direct Apply
Key Skills:
Program Management
Bioinformatics
Data Science

Compensation

Salary Range

$120K - 160K a year

Responsibilities

Manage scientific programs within bioinformatics software development, translating strategy into project roadmaps and supporting regulated releases.

Requirements

8+ years scientific experience with bachelor's degree in computational field, 3+ years managing bioinformatics software programs, familiarity with project tools like Jira, and preferred advanced degrees and regulatory experience.

Full Description

Labcorp is seeking a US remote Senior Scientific Program Manager – Sample to Answer Platform to join our team! (This position is not eligible for visa sponsorship). Job Responsibilities: The Sample to Answer (S2A) research, development, and operational platform is dedicated to generating high-quality clinical results at scale and advancing the use of genetic information in healthcare. The platform supports development needs from across the organization, including Commercial Product, Operations, Regulatory, and IT / software engineering. Reporting to the Senior Manager of Product Operations, this Scientific Program Manager will support the planning, execution, and delivery of development programs, working most closely with the bioinformatics teams. Drive end‑to‑end execution of scientific programs: Manage timelines, milestones, risk mitigation, and cross‑team dependencies for multiple programs. Partner closely with bioinformaticians, data scientists, clinical informaticians, software engineers, and other teams across the S2A platform to translate scientific goals into actionable development plans and ensure smooth delivery across the pipeline lifecycle. Manage a high volume of concurrent bioinformatics projects: Oversee programs spanning pipeline development, algorithm updates, infrastructure modernization, and related computational initiatives. Maintain clarity on priorities, resource constraints, and technical interdependencies while ensuring timely progress across different scientific domains and project maturity levels. Translate scientific and technical strategy into executable project roadmaps: Collaborate with Engineering Managers and Product Managers to convert high‑level scientific objectives into detailed, measurable project plans, including build requirements, stage gate decisions, release criteria, and communication frameworks across teams. Support regulated bioinformatics releases: Coordinate verification and validation activities for updates to analysis pipelines, tooling, and reference data. Develop or contribute to analytical validation plans, change control documentation, release notes, and other documentation for CLIA/CAP and other regulatory environments. Build and refine workflows and processes to increase project execution efficiency: Continuously improve program management systems that support reproducibility, quality, and efficiency within bioinformatics. Enhance processes for dependency tracking, cross‑team communication, decision logging, and standardized documentation across the Sample to Answer platform. Minimum Qualifications: 8 years of laboratory, scientific experience with a bachelor’s degree in bioinformatics, genetics, or computational biology. 3 years or more experience managing interdependent bioinformatics software programs, including pipeline development, versioning, infrastructure modernization, or algorithm validation. 3 years or more experience with program and documentation tools such as Jira, Confluence, Smartsheet, Monday.com used for dependency tracking, release planning, and technical documentation. Preferred Qualifications: 6 years of scientific experience with a Master's degree in bioinformatics, computational biology, or genetics or 3 years of scientific experience with a PhD in bioinformatics, computational biology, or genetics . 3 years or more experience with CLIA/CAP for computational pipelines supporting laboratory‑developed tests (LDTs) 3 years or more experience preparing or reviewing verification and validation documentation for bioinformatics software, algorithm updates, and pipeline releases 3 years or more of Next Generation Sequencing (NGS) bioinformatics, including alignment, variant calling, QC metrics, annotation frameworks, benchmarking approaches, and reference genome/version management 2 years or more experience with data management and SQL queries 2 years or more experience with workflow orchestration and scientific infrastructure Additional Job Standards: Experience working directly with software engineers, bioinformaticians, data scientists, and DevOps/cloud teams on scientific software or computational pipeline development Demonstrated ability to operate in a high‑context‑switching environment, navigating between strategic planning, technical deep dives, and day‑to‑day program execution across multiple computational initiatives. Strong cross‑functional collaboration skills, with the ability to integrate perspectives from science, engineering, QA/RA, product, and operations, and influence outcomes without direct authority. Excellent organizational, communication, and technical translation skills, including the ability to explain complex computational or algorithmic details to non‑technical stakeholders. At Labcorp, we advance science, technology and innovation and recognized as one of the most respected companies in the world. Our team is driven by an energizing purpose to improve health and improve lives. Application window open through: 03/03/2026 Pay Range: $120k-$160k annually (USD) All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers. 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. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. 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 If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. We believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care.

This job posting was last updated on 3/1/2026

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