The Client Solutions Partner manages and grows a portfolio of oncology accounts by driving the adoption of testing solutions and ensuring clinical workflow integration. They serve as the primary point of contact for key stakeholders to optimize care delivery and achieve revenue growth targets.
The role involves reviewing correspondence requests to process invoices, adjustments, and claim updates within the billing system. The coordinator is also responsible for maintaining professional email communication with internal and external customers while ensuring data accuracy in large spreadsheet files.
The Contract Associate II manages the full lifecycle of vendor agreements, including drafting, negotiating, and ensuring compliance with company standards. This role also serves as a liaison between the Law Department, Procurement, and business stakeholders to align contracts with operational needs.
The representative acts as a liaison between LabCorp, customers, and patients to resolve inquiries and provide technical information regarding lab services. They are responsible for maintaining accurate records, reviewing test forms for accuracy, and ensuring high levels of customer satisfaction.
Act as a liaison between LabCorp, customers, and patients to resolve inquiries and provide test results. Maintain accurate records and CRM data while ensuring compliance with HIPAA and internal quality standards.
The representative acts as a liaison between LabCorp, customers, and patients to resolve inquiries and provide accurate test results. They are responsible for maintaining accurate records, troubleshooting technical issues, and ensuring high standards of customer satisfaction.
The representative acts as a liaison between Labcorp, customers, and patients to resolve inquiries and provide accurate test results. They are responsible for maintaining accurate CRM data, troubleshooting technical issues, and ensuring high standards of customer satisfaction.
Serve as a liaison among Labcorp, physician offices, hospital laboratories, patients, and internal customers by answering inquiries, providing test information and results, and resolving routine or complex issues. Review test forms, maintain accurate HIPAA-compliant records, troubleshoot basic technical problems, and meet customer service, quality, and productivity standards.
The Data Manager acts as the primary contact for clinical studies, managing data transfer strategies and ensuring data quality from start-up through database lock. They serve as a liaison between cross-functional teams and maintain audit-ready documentation in compliance with regulatory requirements.
Performs routine high complexity analyses and interpretations of flow cytometry dot plots for leukemia and lymphoma specimens. Ensures quality control, documentation, and prioritization of cases while assisting in the training of laboratory personnel.
The IT Operations Coordinator II manages user access requests, system security administration, and compliance activities across various enterprise applications. They also support operational reporting, audit evidence preparation, and the development of standard operating procedures to ensure efficient technology operations.
The analyst performs routine high-complexity flow cytometry analyses and interpretations for leukemia and lymphoma specimens. They are also responsible for maintaining quality control documentation, prioritizing cases, and assisting in the training of laboratory personnel.
The Manager will partner with stakeholders to identify opportunities for leveraging enterprise data and design scalable reporting and analytical solutions. They will also lead the development of dashboards, maintain semantic models, and mentor junior team members while applying AI-assisted development practices.
The Clinical Trials Monitor II develops and manages study-specific supply strategies to ensure clinical trial kits are available while minimizing waste. They act as a client-facing subject-matter expert, collaborating with cross-functional teams to identify risks and make data-informed decisions.
The Study Coordinator will manage study activities including protocol preparation, milestone tracking, and ensuring compliance with regulatory guidelines and SOPs. They will also facilitate communication across global teams and perform quality control on scientific reports and data.
The analyst is responsible for monitoring clinical study laboratory metrics, identifying study risks, and developing mitigation plans. They also create customized monitoring packages and provide actionable insights to internal and external stakeholders.
The Study Coordinator will manage study activities, including protocol preparation, milestone tracking, and ensuring compliance with regulatory guidelines and SOPs. They will also facilitate communication across global teams and perform quality control on scientific reports and data.
Achieve sales targets by developing client relationships, prospecting for new business, managing accounts and opportunities, and accurately forecasting the sales pipeline. Lead client presentations and proposals, coordinate with internal teams to win multi-unit projects, and provide regular activity reports and competitive insights.
The Global Monitor is responsible for identifying clinical study risks, developing mitigation plans, and monitoring laboratory metrics to ensure study health. They also create customized monitoring packages and present actionable data insights to internal and external stakeholders.
The Clinical Trials Monitor II develops and manages study-specific supply strategies to ensure clinical trial kits are available while minimizing waste. They act as a client-facing subject-matter expert, identifying risks and making data-informed decisions to optimize study operations.
The Global Study Manager acts as the primary liaison between clients and the Labcorp study team to ensure seamless study delivery. They are responsible for project management oversight, including budget, risk, and milestone management across a portfolio of clinical studies.
The Global Study Manager acts as the primary liaison between clients, CROs, and internal teams to ensure seamless study delivery. They are responsible for project management oversight, including budget, risk, and milestone management across a portfolio of global and local clinical studies.
The Global Study Manager acts as the primary liaison between clients and the Labcorp study team to ensure seamless study delivery. They are responsible for project management oversight, including budget, risk, and milestone management across a portfolio of global and local clinical studies.
The Global Study Manager acts as the primary liaison between clients, CROs, and internal teams to ensure seamless study delivery. They provide project management oversight, including budget, risk, and milestone management for a portfolio of global and local clinical studies.
The Clinical Trials Monitor II develops and manages study-specific supply strategies to ensure clinical trial kits are available while minimizing waste. They act as a client-facing subject-matter expert to identify risks, provide data-informed recommendations, and coordinate across global teams.
Create and update digital sales training materials, including courses, presentations, webinars, assessments, podcasts, videos, and animations. Collaborate with trainers, marketing, content managers, and subject matter experts to turn complex information into engaging learning resources and support digital learning platforms.
The Flow Cytometry Analyst I is responsible for performing accurate patient sample analysis using specialized software and established laboratory procedures. They also support technical transfers and ensure all data documentation meets rigorous quality and regulatory standards.
The Study Design Lead is responsible for interpreting sponsor protocol requirements to generate Statements of Work and designing protocol-specific databases. They act as a consultant to clients and internal teams, managing study risks, budget impacts, and coordinating internal processes to ensure high-quality study delivery.
The Study Design Lead is responsible for interpreting sponsor protocol requirements to generate Statements of Work and designing protocol-specific databases. They act as a consultant to internal and external stakeholders to assess study feasibility, manage risks, and ensure high-quality study design execution.
The Study Design Lead is responsible for interpreting sponsor protocol requirements to generate Statements of Work and comprehensive database designs. They act as a consultant to internal and external stakeholders, managing study risks, budget impacts, and project feasibility.
The Study Design Lead is responsible for interpreting sponsor protocol requirements to generate Statements of Work and designing protocol-specific databases. They act as a consultant to clients and internal teams, managing study risks, budget impacts, and coordinating internal feasibility and supply processes.
Manage national accounts to achieve revenue growth and drive C-suite level sales with value-based care networks. Collaborate with internal teams to develop product programs and lead sales implementations across regional teams.
The QA Engineer will analyze business requirements and user stories to develop comprehensive test plans and automated test cases for Salesforce and enterprise applications. They will collaborate with cross-functional teams to execute functional, integration, and regression testing while ensuring high software quality standards.
The role involves notifying investigator sites and sponsors of laboratory results and test cancellations while monitoring and resolving accession holds. You will also act as a liaison for internal and external clients, ensuring project-related questions are addressed via phone and email.
The role involves notifying investigator sites and sponsors of laboratory results and test cancellations while monitoring and resolving accession holds. The assistant will also act as a liaison for clients, support project-related inquiries, and ensure patient safety protocols are strictly followed.
The Global Study Manager acts as the primary liaison between clients, CROs, and internal teams to ensure seamless study delivery and project oversight. They are responsible for managing a portfolio of complex global studies, including budget, risk, and milestone management while maintaining high standards of client service.
The Regional Manager will oversee regional sales and account management functions to drive growth within the clinical segment. They are responsible for leading a team of sales representatives, developing revenue generation strategies, and maintaining high-level relationships with key accounts.
The Staff Software Engineer will own and deliver product or platform goals across multiple years and teams, while mentoring and guiding experienced engineers. They will influence the roadmaps of other teams and ensure adherence to best practices in system design and architecture.
The Sr. Director is responsible for aligning and integrating initiatives to accelerate CGT commercial growth across BLS. This role involves collaborating across a matrixed organization to enhance CGT capabilities and foster partnerships for business expansion.
The Sr. Director is responsible for aligning and integrating initiatives to accelerate CGT commercial growth across BLS. This role involves collaborating with internal stakeholders and enhancing CGT capabilities to foster partnerships and drive business expansion.
The Sr. Director is responsible for aligning and integrating initiatives to accelerate CGT commercial growth across BLS. This role involves collaborating across a matrixed organization to enhance CGT capabilities and foster partnerships for business expansion.
The Senior Software Engineer will leverage scientific and technical knowledge to support genetic scientists in identifying relevant information and decision-making in R&D projects. They will also establish and automate a knowledge extraction pipeline for scientific literature.
Leverage scientific domain and technical knowledge to support genetic scientists in identifying relevant information and decision-making in R&D projects. Collaborate with internal teams to design and implement solutions that meet stakeholder requirements.
The Staff Software Engineer will own and deliver product or platform goals across multiple years and teams while mentoring and guiding experienced engineers. They will influence the roadmaps of other teams and ensure adherence to best practices in system design and architecture.
