MRD-Specific Responsibilities * Define and execute the MRD portfolio strategy and roadmap across clinical use cases, technology platforms, and market evolution. * Translate emerging clinical evidence ...
MRD-Specific Responsibilities * Define and execute the MRD portfolio strategy and roadmap across clinical use cases, technology platforms, and market evolution. * Translate emerging clinical evidence ...
MRD-Specific Responsibilities * Define and execute the MRD portfolio strategy and roadmap across clinical use cases, technology platforms, and market evolution. * Translate emerging clinical evidence ...
MRD-Specific Responsibilities * Define and execute the MRD portfolio strategy and roadmap across clinical use cases, technology platforms, and market evolution. * Translate emerging clinical evidence ...
MRD-Specific Responsibilities * Define and execute the MRD portfolio strategy and roadmap across clinical use cases, technology platforms, and market evolution. * Translate emerging clinical evidence ...
MRD-Specific Responsibilities * Define and execute the MRD portfolio strategy and roadmap across clinical use cases, technology platforms, and market evolution. * Translate emerging clinical evidence ...
You will support assay development and clinical validation by assisting in experimental design, data collection and analysis with scientists to advance our MRD assay. The role requires a bachelor ...
New
You will support assay development and clinical validation by assisting in experimental design, data collection and analysis with scientists to advance our MRD assay. The role requires a bachelor ...
New
In this role, you will support assay development and clinical validation, assist in experimental design, data collection and analysis, and collaborate with scientists to advance our MRD assay. You ...
New
In this role, you will support assay development and clinical validation, assist in experimental design, data collection and analysis, and collaborate with scientists to advance our MRD assay. You ...
New
Head of Business Development
Milpitas, CA · On-site
The successful candidate will build and manage a robust deal pipeline while helping shape AccuScan's commercialization strategy for its MRD portfolio. This leader will play a key role in accelerating ...
Head of Business Development
Milpitas, CA · On-site
The successful candidate will build and manage a robust deal pipeline while helping shape AccuScan's commercialization strategy for its MRD portfolio. This leader will play a key role in accelerating ...
The successful candidate will build and manage a robust deal pipeline while helping shape AccuScan's commercialization strategy for its MRD portfolio. This leader will play a key role in accelerating ...
The successful candidate will build and manage a robust deal pipeline while helping shape AccuScan's commercialization strategy for its MRD portfolio. This leader will play a key role in accelerating ...
Head of Business Development
Milpitas, CA · On-site
The successful candidate will build and manage a robust deal pipeline while helping shape AccuScan's commercialization strategy for its MRD portfolio. This leader will play a key role in accelerating ...
Quick apply
Head of Business Development
Milpitas, CA · On-site
The successful candidate will build and manage a robust deal pipeline while helping shape AccuScan's commercialization strategy for its MRD portfolio. This leader will play a key role in accelerating ...
The CDM will play a critical role in supporting clinical data pipelines, investigating anomalies, and driving MRD-focused analyses, pipeline improvements, and research initiatives. Clinical Data ...
The CDM will play a critical role in supporting clinical data pipelines, investigating anomalies, and driving MRD-focused analyses, pipeline improvements, and research initiatives. Clinical Data ...
Director of Product Management
Milpitas, CA · On-site
$271K - $284K/yr
Define the product roadmap for MRD assays across multiple indications. * Translate clinical data into product requirements, claims, and market positioning. * Support regulatory and reimbursement ...
Director of Product Management
Milpitas, CA · On-site
$271K - $284K/yr
Define the product roadmap for MRD assays across multiple indications. * Translate clinical data into product requirements, claims, and market positioning. * Support regulatory and reimbursement ...
Director of Product Management
Milpitas, CA · On-site
$271K - $284K/yr
Define the product roadmap for MRD assays across multiple indications. * Translate clinical data into product requirements, claims, and market positioning. * Support regulatory and reimbursement ...
Director of Product Management
Milpitas, CA · On-site
$271K - $284K/yr
Define the product roadmap for MRD assays across multiple indications. * Translate clinical data into product requirements, claims, and market positioning. * Support regulatory and reimbursement ...
Clinical Data Manager
Milpitas, CA · On-site
The CDM will play a critical role in supporting clinical data pipelines, investigating anomalies, and driving MRD-focused analyses, pipeline improvements, and research initiatives. Clinical Data ...
Quick apply
Clinical Data Manager
Milpitas, CA · On-site
The CDM will play a critical role in supporting clinical data pipelines, investigating anomalies, and driving MRD-focused analyses, pipeline improvements, and research initiatives. Clinical Data ...
Clinical Data Manager
Milpitas, CA · On-site
The CDM will play a critical role in supporting clinical data pipelines, investigating anomalies, and driving MRD-focused analyses, pipeline improvements, and research initiatives. Clinical Data ...
Clinical Data Manager
Milpitas, CA · On-site
The CDM will play a critical role in supporting clinical data pipelines, investigating anomalies, and driving MRD-focused analyses, pipeline improvements, and research initiatives. Clinical Data ...
Director of Product Management
Milpitas, CA · On-site
$271K - $284K/yr
Define the product roadmap for MRD assays across multiple indications. * Translate clinical data into product requirements, claims, and market positioning. * Support regulatory and reimbursement ...
Quick apply
Director of Product Management
Milpitas, CA · On-site
$271K - $284K/yr
Define the product roadmap for MRD assays across multiple indications. * Translate clinical data into product requirements, claims, and market positioning. * Support regulatory and reimbursement ...
Archaeologist I
$49K - $58K/yr
The employee will also manage equipment and act as a dive safety officer for the MRD. Job Related Minimum Required Education and Experience * Requires a bachelor's degree in area of research ...
Archaeologist I
$49K - $58K/yr
The employee will also manage equipment and act as a dive safety officer for the MRD. Job Related Minimum Required Education and Experience * Requires a bachelor's degree in area of research ...
Product Manager
Los Angeles, CA · On-site
MRD's, road map crequirements) to drive each phase in the lifecycle. • Communicatekey solution messages (e. g. positioning, value proposition, features/benefits)to customers, prospects, and ...
Product Manager
Los Angeles, CA · On-site
MRD's, road map crequirements) to drive each phase in the lifecycle. • Communicatekey solution messages (e. g. positioning, value proposition, features/benefits)to customers, prospects, and ...
Product Manager
Los Angeles, CA · On-site
MRD's, road map crequirements) to drive each phase in the life cycle Communicate key solution messages (e. g. positioning, value proposition, features/benefits) to customers, prospects, and internal ...
Product Manager
Los Angeles, CA · On-site
MRD's, road map crequirements) to drive each phase in the life cycle Communicate key solution messages (e. g. positioning, value proposition, features/benefits) to customers, prospects, and internal ...
Project Manager
Pleasanton, CA · On-site
Work with Engineering to facilitate and manage the decomposition of the MRD into engineering requirements, generation of design concepts, trade-off analysis and down-selection of concepts ...
Project Manager
Pleasanton, CA · On-site
Work with Engineering to facilitate and manage the decomposition of the MRD into engineering requirements, generation of design concepts, trade-off analysis and down-selection of concepts ...
Project Manager
Pleasanton, CA · On-site
Work with Engineering to facilitate and manage the decomposition of the MRD into engineering requirements, generation of design concepts, trade-off analysis and down-selection of concepts ...
Project Manager
Pleasanton, CA · On-site
Work with Engineering to facilitate and manage the decomposition of the MRD into engineering requirements, generation of design concepts, trade-off analysis and down-selection of concepts ...
Research Associate
Milpitas, CA · On-site
You will assist in experimental design, data collection, and analysis while collaborating with scientists to advance our MRD assay. Responsibilities: * Receive and process specimen shipments
Research Associate
Milpitas, CA · On-site
You will assist in experimental design, data collection, and analysis while collaborating with scientists to advance our MRD assay. Responsibilities: * Receive and process specimen shipments
Mrd information
See California salary details
$89.68 - $90.52
4% of jobs
$90.52 - $91.36
15% of jobs
$91.78 is the 25th percentile. Wages below this are outliers.
$91.36 - $92.20
12% of jobs
$92.20 - $93.04
16% of jobs
The median wage is $93.27 / hr.
$93.04 - $93.88
12% of jobs
$93.88 - $94.72
16% of jobs
$94.77 is the 75th percentile. Wages above this are outliers.
$94.72 - $95.56
9% of jobs
$95.56 - $96.40
5% of jobs
$96.40 - $97.25
3% of jobs
$97.25 - $98.09
5% of jobs
$98.09 - $98.93
3% of jobs
$89
$93
$98
How much do mrd jobs pay per hour?
What are MRDs (Medical Records Directors)?
What jobs can you do with an MD but no residency?
What is the difference between Mrd vs Radiologic Technologist?
| Aspect | Mrd | Radiologic Technologist |
|---|---|---|
| Required Credentials | Associate's degree, certification in MRI technology | Associate's degree, certification in radiography |
| Work Environment | Hospitals, imaging centers, clinics | Hospitals, outpatient clinics, diagnostic labs |
| Industry Usage | Specialized in MRI procedures | General radiography and imaging |
| Common Search/Comparison | Yes | Yes |
The main difference between Mrd and Radiologic Technologist lies in their specialization. Mrd professionals focus specifically on MRI imaging, requiring specialized training and certification, while Radiologic Technologists perform a broader range of imaging procedures like X-rays. Both roles work in similar healthcare environments, but Mrd specialists have a narrower focus on MRI technology.
What is a MRR job?
What are the key skills and qualifications needed to thrive as a Medical Records Director (MRD), and why are they important?
What holistic job makes the most money?
What jobs pay 500,000 a year in the US?

$274K - $287K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 12 days ago
Labcorp rating
6.6
Based on 1,133 frontline employees who took The Breakroom Quiz
97th of 120 rated laboratories
Job description
Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world's most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you'll have the opportunity to do meaningful work, grow your career and make a real impact on people's health around the world. Together, we're improving health and improving lives.
Director, Product Management, Oncology, Molecular Residual Disease (MRD)
Labcorp is seeking a Director, Product Management, Oncology, Molecular Residual Disease (MRD), to join our Oncology Product Team.
Responsibilities:
Core Responsibilities
Lead portfolio strategy and lifecycle management, including roadmap development, forecasting, and performance optimization from concept through commercialization and scale.
Apply deep disease expertise, regulatory insight, and business acumen to drive adoption, profitability, and sustained portfolio growth.
Monitor scientific, regulatory, and competitive trends to inform strategic direction and investment priorities.
Develop robust business cases encompassing market opportunity, segmentation, financial projections, operating models, and product requirements.
Serve as the commercial lead across R&D, Operations, and Market Access, ensuring alignment on product strategy, pricing, and go-to-market approach.
Represent the voice of the customer in governance and planning forums, incorporating insights into prioritization and product evolution.
Drive strategic partnerships that enhance product capabilities, expand access, and create new revenue opportunities.
Partner with Product and Customer Marketing to support differentiation, positioning, and thought leadership.
Ensure operational readiness for launches, enhancements, and acquisitions, including workflow design and execution.
Analyze utilization, access, and performance metrics to continuously improve product outcomes and inform leadership decisions.
Collaborate with Commercial, Medical Affairs, and Scientific teams on field enablement, evidence generation, and customer engagement.
Own portfolio KPIs and provide ongoing insights on growth, expansion, and optimization opportunities.
MRD-Specific Responsibilities
Define and execute the MRD portfolio strategy and roadmap across clinical use cases, technology platforms, and market evolution.
Translate emerging clinical evidence, clinical trials, and guideline updates into actionable product strategies.
Establish MRD use cases spanning treatment monitoring, recurrence detection, adjuvant decision-making, and clinical trial integration.
Partner with Operations to design scalable workflows that optimize performance. turnaround time and deliver a seamless ordering-to-reporting experience.
Collaborate with Market Access to develop reimbursement strategies and expand coverage for emerging indications.
Work with Medical Affairs and Science to shape evidence generation and publication strategies supporting clinical adoption and payer access.
Engage biopharma team to support external studies and trial-based applications.
Define and track key metrics such as adoption by line of therapy, longitudinal utilization, turnaround time, and payer coverage.
Build and maintain strong relationships with key opinion leaders, academic institutions, and oncology networks.
Minimum Qualifications:
Bachelor's degree in Molecular Biology, Life Sciences or Bioengineering.
7 or more years experience in product management or portfolio strategy.
7 or more years experience in diagnostics, pharmaceuticals, or life sciences.
5 or more years managing diagnostic services or oncology testing products.
Preferred Qualifications:
3 or more years experience in circulating tumor DNA (ctDNA), NGS, or oncology diagnostics.
2 or more years experience with MRD, liquid biopsy, or longitudinal testing.
Advanced degree in Molecular Biology, Oncology or Life Sciences.
Master's degree in Business Administration (MBA).
Additional Job Standards:
Experience with diagnostics commercialization and regulatory pathways.
Experience with market access/payor policies for diagnostics.
Forecasting and pricing experience.
Demonstrated success launching and scaling regulated diagnostic products.
Up to 20% travel for customer engagement, scientific meetings, advisory boards, and conferences.
Skills and Competencies
Strategic thinking
Cross functional leadership
Product lifecycle management & commercialization
Scientific and clinical fluency
Analytical and forecasting capability
Stakeholder influence
Operational and financial acumen
Competitive insight
Strong product strategy and lifecycle management capability
Deep understanding of oncology clinical workflows and treatment paradigms
Technical fluency in ctDNA, NGS technologies, and assay performance tradeoffs
Knowledge of U.S. diagnostic reimbursement and access pathways
Strong analytical, financial modeling, and storytelling skills
Proven ability to lead cross functional teams without direct authority
Comfort engaging external oncologists, pathologists, and scientific leaders
Ability to operate in areas of clinical and regulatory uncertainty
About the Role
As a global leader in diagnostic services, Labcorp is committed to improving health and improving lives. Diagnostic Marketing plays a central role as a commercial partner, driving access to innovative testing solutions, strengthening leadership in specialized diagnostics, advancing digital capabilities, and enhancing customer experience to support sustainable growth.
Within this function, the Director of Product Management is responsible for portfolio strategy, commercialization, and lifecycle execution to ensure strong product performance and successful launches. The role aligns cross-functional stakeholders and represents the commercial perspective across R&D, Operations, and Market Access. It also leads forecasting, resource planning, and operational efficiency, translating market insights into strategic decisions that expand margins, improve competitiveness, and drive profitable growth.
The Director, Oncology (MRD) leads the strategy and lifecycle management of Labcorp's molecular residual disease (MRD) portfolio. This includes advancing differentiated solutions that enable treatment monitoring, early detection of recurrence, and ongoing cancer management across solid tumors and hematologic malignancies.
This role translates evolving clinical evidence, emerging technologies (including tumor-informed and tumor-naive approaches), payer dynamics, and competitive trends into actionable strategies that drive adoption and access. Working cross-functionally with Science, Medical Affairs, Product Marketing, Commercial Strategy, Market Access, IT, and Operations, the Director ensures seamless, best-in-class customer experience from test ordering through reporting.
The position also requires close collaboration with oncologists, pathologists, translational researchers, and MRD thought leaders, as well as engagement with biopharma partners to support therapy-specific applications and clinical trial integration.
The candidate must reside in New York (NY), California (CA), or North Carolina (NC), located near a Labcorp hub. Applicants who live within 35 miles of either the Burlington, NC or Durham, NC location will follow a hybrid schedule, which includes a minimum of three in-office days per week at an assigned location-either Burlington or Durham-supporting both collaboration and flexibility.
Application Window: Application window will close on August 17, 2026.
Pay Range $170,000 - $190,000 annually + annual bonus eligibility
All job offers will bebased on a candidate's skills and prior relevant experience, applicabledegrees/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.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 toworka 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, pleaseclick here.
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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 ouraccessibility siteor contact us atLabcorp Accessibility. Formore information about how we collect and store your personal data, please see ourPrivacy Statement.
About Labcorp
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Burlington, NC, US
Year founded
1978