Qureos Mentor

Caris Life Sciences

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary 
This position is responsible for equipment compliance with all applicable regulatory requirements. This role ensures adherence to Good Documentation Practices (GDP) in all paper and electronic records generated within asset lifecycle management for all managed equipment and assets. This includes assisting with the authoring and review of instrument reports, facilitation of corrections per GDP, ensuring data integrity across laboratory instrumentation records in applicable electronic platforms, and performing final quality signoff for work orders and verifications. 
 
Job Responsibilities<ul><li>
Ensure equipment verification record compliance with all applicable regulatory requirements (CLIA, NYS, CAP, ISO, FDA, IVDR, etc.).</li><li>
Collaborate and assist in clinical requalification of instrumentation to maintain company-wide regulatory compliance and operational efficiency.</li><li>
Author cross-correlation reports for Molecular, IHC and liquid profiling workflows.</li><li>
Ensure requalification paperwork is reviewed and approved in a timely fashion.</li><li>
Review records for accuracy and Good Documentation Practices (GDP).</li><li>
Analyze system/process dependencies between laboratory instrumentation, operations, IT infrastructure, and Quality to define and execute projects within the validation programs.</li><li>
Participate in internal and external audits with tasks such as audit preparation, answering questions, and providing documentation to auditors.</li><li>
Support asset lifecycle management activities.</li><li>
Author, review, revise, and implement standard operating procedures (SOPs).</li><li>
Manage company records in accordance with regulatory requirements and company policies.</li><li>
Engage in cross-functional collaborations between Systems Engineering, Laboratory, IT, Software QA, and Quality teams to support program alignment between organizational and regulatory requirements.</li></ul> 
Required Qualifications<ul><li>
Bachelor's degree in engineering, biological science, computer science, or similar field</li><li>
Strong knowledge of QMS requirements per CAP/CLIA, ISO 13485, and 21 CFR Part 820.</li><li>
One year of experience working in a regulated laboratory environment.</li><li>
Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use.</li></ul> 
Preferred Qualifications<ul><li>
Lean Six Sigma certified.</li><li>
Two years of experience working in a regulated laboratory environment with a focus on laboratory instrumentation and equipment.</li><li>
Master's degree in engineering, biological science, computer science, or similar field.</li></ul> 
Physical Demands<ul><li>
Employee must be able to use standard office equipment.</li><li>
Employee must have ability to sit and stand for extended periods of time.</li><li>
Work is split between desk/cubicle environment and laboratory environment. Employee may have exposure to high noise levels, fumes, and biohazardous materials in the laboratory environment.</li></ul> 
Training<ul><li>
All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.</li></ul> 
Other<ul><li>
This position requires some evenings, weekends and/or holidays.</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Systems Engineering Analyst

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary
The Alliance Manager is responsible for leading the coordination, execution, and relationship management of projects partnering with biopharma and biotech companies.
Job Responsibilities
<ul><li>Work closely with biopharma business development, clinical operations, data integration, quality, product development, bioinformatics/translational sciences, and regulatory affairs to develop and implement CDx programs from proof of concept through completion of approved on-market therapeutics, blood/tissue molecular profiling and data programs, and real-world evidence/data/insights/target discovery programs.</li><li>
Directly manage a portfolio of alliances.</li><li>
Lead partner implementations in a way that exceeds partner expectations and meets timelines.</li><li>
Manage project functions relating to deliverables, budgets, revenue, and proposals.</li><li>
Effectively research and communicate the value of Caris offerings and deliver scientific information in a manner that is appropriate for the intended audience, and leverage subject matter experts appropriately.</li><li>
Conduct due diligence to gain a thorough understanding of partner's organization and objectives.</li><li>
Develop and demonstrate strong competency in Caris's solutions to provide best practice recommendations to our partners.</li><li>
Build and maintain strong customer relationships through partner focus, professional demeanor, reliability, and responsiveness.</li><li>
Utilize laboratory information system and customer relationship management software to enter, gather, and analyze data regarding study health and study management.</li><li>
Evaluate client concerns, complaints, and trends to recommend changes to accommodate client needs.</li><li>
Work closely with R &amp; D leaders, clinical operations, quality, and regulatory affairs on the proof of concept of the diagnostic assay in clinical trials.</li><li>
Lead partner meetings and workshops, ensuring decisions and action items are clearly documented and tracked to completion.</li></ul>
Required Qualifications<ul><li>
Bachelor's Degree in relevant field(s) of study such as healthcare administration/policy, drug development, clinical research, oncology/nursing/clinical, science/bioinformatics or equivalent professional experience.</li><li>
2+ years of experience in one or more of the following: molecular biology, clinical molecular diagnostics, or oncology, writing/utilizing scientific protocols and proposals, oncology/pathology/lab workflow, clinical research, including regulations, phases, clinical protocols, scientific concepts, or study management, implementing projects in the healthcare space, or drug development or companion diagnostics.</li><li>
Strong background in managing multiple projects simultaneously.</li><li>
History of delivering results on time within a multi-group setting.</li><li>
Proficiency in medical and healthcare terminology.</li><li>
Ability to travel up to 20%.</li></ul>
Preferred Qualifications<ul><li>
Skills in Microsoft Word, Excel, PowerPoint, Visio, and/or project management software, e.g., MS Project or Jira.</li><li>
Awareness and understanding of emerging trends and technologies in healthcare, oncology/pathology, and/or molecular testing.</li><li>
Awareness about compliance to applicable regulatory standards, particularly CLIA, GMP, and GCP.</li><li>
Professional certification in area of expertise, e.g., PMP, CCRA, RN, etc., or participation in nationally recognized organizations (reference bullet above).</li><li>
Highly self-motivated, self-directed, and attentive to detail.</li><li>
Ability to work in a complex and matrix team environment; experience working in a team-oriented, collaborative environment.</li><li>
Detail-oriented, proven problem solver and analytical thinker with strong organizational and conflict resolution skills.</li><li>
The ability to communicate technical information in a clear, concise, and effective manner.</li><li>
Able to work effectively with, influence, and lead employees at different levels of the organization using strong interpersonal skills, collaboration, and teamwork.</li><li>
Proven abilities in leading complex problem management and process analysis.</li><li>
Ability to handle multiple tasks, set priorities, schedule, and meet deadlines.</li><li>
Strong interpersonal and relationship-building skills, with the ability to manage up, down and across levels of the organization.</li><li>
Continuous learner with a desire to improve on existing processes to achieve higher degrees of partner success and improved quality and operational efficiencies.</li></ul>
Physical Demands<ul><li>
Will work at a computer most of the time.</li><li>
Must possess ability to sit and/or stand for long periods of time.</li><li>
Must possess ability to perform repetitive motion.</li><li>
Ability to lift 25 pounds.</li></ul>
Training<ul><li>
All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.</li></ul>
Other
<ul><li>This position requires periodic travel and some evenings, weekends and/or holidays.</li></ul>
Annual Hiring Range
$125,000 - $155,000
Actual compensation offer to candidate may vary from posted hiring range based upon geographic location, work experience, education, and/or skill level. The pay ratio between base pay and target incentive (if applicable) will be finalized at offer. 
Description of Benefits<ul><li>
Highly competitive and inclusive medical, dental and vision coverage options</li><li>
Health Savings Account for medical expenses and dependent care expenses</li><li>
Flexible Spending Account to pay for certain out-of-pocket expenses</li><li>
Paid time off, including: vacation, sick time and holidays</li><li>
401k match and Financial Planning tools</li><li>
LTD and STD insurance coverages, as well as voluntary benefit options</li><li>
Employee Assistance Program</li><li>
Pet Insurance</li><li>
Legal Assistance</li><li>
Tuition Assistance</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Alliance Manager (Remote)

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary 
The Oncology Account Executive is a customer-facing sales professional responsible for driving sustained territory growth through new account acquisition and expansion of existing customer relationships. This role combines strategic prospecting, consultative selling, and high-touch account management to position Caris as the preferred partner for comprehensive tumor profiling solutions. 
 
This position builds strong clinical and operational relationships with oncologists, pathologists, and key healthcare stakeholders. The Account Executive ensures an exceptional customer experience from order initiation through report delivery while supporting adoption and utilization of Caris molecular profiling solutions. The role partners closely with Regional Business Directors, Commercial Leadership, Client Services, and cross-functional teams to execute territory growth strategies. 
 
The ideal candidate will have multiple years of successful sales experience in oncology, diagnostics, medical devices, or pharmaceuticals, with demonstrated strength in consultative selling, account growth, and relationship management. 
 
Job Responsibilities 
Sales &amp; Territory Growth<ul><li>
Drive new account acquisition and organic growth through strategic prospecting, value-based selling, and clinical education.</li><li>
Position Caris as a preferred or sole-source provider of tumor profiling and molecular intelligence solutions.</li><li>
Analyze territory opportunities and develop strategic sales plans to achieve growth objectives.</li><li>
Meet or exceed assigned revenue, activity, and performance targets.</li></ul>
Account Management &amp; Customer Experience<ul><li>
Build and maintain strong customer relationships through consistent in-person engagement.</li><li>
Ensure a seamless customer experience across the full order lifecycle.</li><li>
Maintain open communication with key account stakeholders and escalate issues when satisfaction is at risk.</li><li>
Execute retention strategies and identify upselling and cross-selling opportunities.</li></ul>
Clinical &amp; Technical Expertise<ul><li>
Engage with oncology clinicians and allied teams across clinics, pathology labs, and hospital settings.</li><li>
Support physicians with ordering and interpretation of the CMI platform, including access to PHI when required.</li><li>
Demonstrate and advise on technology solutions such as portals, EMR integrations, and workflows.</li><li>
Maintain strong knowledge of molecular profiling, biomarkers, and competitive offerings.</li></ul>
Business, Reimbursement &amp; Market Insight<ul><li>
Provide consultative guidance on billing, reimbursement, and payer dynamics.</li><li>
Serve as a resource on laboratory reimbursement and operational workflows.</li><li>
Share market trends, customer feedback, and competitive insights with leadership.</li></ul>
Collaboration &amp; Administration<ul><li>
Collaborate with Client Services, Regional Business Directors, and Commercial Leadership.</li><li>
Maintain accurate CRM documentation and complete required administrative tasks.</li><li>
Maintain assigned company assets.</li><li>
Support meetings, conferences, and trade shows as required.</li><li>
Perform other duties as assigned.</li></ul> 
Required Qualifications<ul><li>
Bachelor&rsquo;s degree required.</li><li>
Minimum of 3 years of relevant sales experience.</li><li>
Strong understanding of oncology practices and molecular diagnostics.</li><li>
Knowledge of billing and reimbursement environments.</li><li>
Excellent communication and relationship-building skills.</li><li>
Ability to manage multiple priorities in a matrixed environment.</li><li>
Proficiency with Microsoft Office and CRM tools.</li><li>
Valid driver&rsquo;s license and willingness to travel regularly.</li><li>
Successful completion of pre-employment requirements.</li></ul> 
Preferred Qualifications<ul><li>
5+ years of sales experience with oncology or molecular diagnostics focus.</li><li>
Established oncology or pathology relationships.</li><li>
Familiarity with hospital systems and pathology networks.</li></ul> 
Physical Demands<ul><li>
Ability to sit or stand for extended periods.</li><li>
Ability to lift routine office materials.</li></ul> 
Additional Information<ul><li>
Travel required, including possible evenings, weekends, or holidays.</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Oncology Account Executive - Arkansas West

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary 
The National Account Molecular Science Liaison (MSL) is a field-based scientific expert within Medical Affairs responsible for developing and executing strategic scientific engagement across Caris' largest national oncology networks, integrated delivery networks (IDNs), government healthcare systems, and other strategic enterprise accounts. 
Reporting to the Director, National Account Molecular Science Liaisons, this role serves as the primary scientific liaison to executive clinical leadership, precision medicine committees, medical directors, pathway leaders, and other key stakeholders. The National Account MSL collaborates closely with Medical Affairs leadership and cross-functional teams to develop enterprise scientific strategies, support implementation of molecular profiling programs, and align national account objectives with field medical execution. This position plays a key role in advancing precision oncology initiatives, strengthening scientific partnerships, and expanding access to comprehensive molecular profiling across enterprise healthcare organizations. 
 
Job Responsibilities<ul><li>
Serve as the Medical Affairs scientific lead for assigned national oncology networks, integrated delivery networks (IDNs), government healthcare systems, and other strategic enterprise accounts.</li><li>
Develop and execute enterprise scientific engagement strategies aligned with Medical Affairs and organizational priorities.</li><li>
Establish and maintain scientific relationships with executive clinical leadership, precision medicine committees, medical directors, pathway leaders, and multidisciplinary stakeholders.</li><li>
Deliver balanced, evidence-based scientific exchange regarding molecular diagnostics, biomarkers, comprehensive genomic profiling, and precision oncology.</li><li>
Lead and participate in Molecular Tumor Boards (MTBs), scientific advisory meetings, educational programs, and clinical discussions.</li><li>
Translate emerging clinical evidence into meaningful scientific discussions that support patient care and precision medicine adoption.</li><li>
Support enterprise precision medicine initiatives, workflow optimization, biomarker implementation, quality improvement projects, and educational collaborations.</li><li>
Partner with Regional Molecular Science Liaisons and Medical Affairs leadership to align enterprise strategy with regional field execution.</li><li>
Develop enterprise account profiles, stakeholder maps, engagement plans, executive reports, dashboards, and strategic analyses.</li><li>
Collaborate with cross-functional teams including Medical Affairs, Commercial, Market Access, Pathology Operations, Informatics, and Business Development to support coordinated customer engagement.</li><li>
Monitor molecular diagnostics trends, precision oncology advancements, and competitive intelligence, communicating relevant insights to Medical Affairs leadership.</li><li>
Represent Caris Medical Affairs at national, regional, enterprise, and government scientific meetings, advisory boards, and educational programs.</li><li>
Support scientific engagement with Veterans Affairs (VA), Department of Defense (DoD), and other government healthcare systems, as assigned.</li><li>
Perform other duties as assigned.</li></ul> 
Required Qualifications<ul><li>
Advanced clinical or scientific degree (MD, DO, PharmD, PhD, DNP, NP, PA, or equivalent).</li><li>
Minimum of five (5) years of Oncology Medical Affairs, Molecular Science Liaison, or equivalent scientific field experience.</li><li>
Demonstrated expertise in oncology, molecular diagnostics, precision medicine, biomarkers, and comprehensive genomic profiling.</li><li>
Experience engaging executive clinical leaders within complex healthcare organizations.</li><li>
Excellent scientific communication, presentation, relationship management, and collaboration skills.</li><li>
Strong organizational, analytical, strategic planning, and project management skills.</li><li>
Ability to travel up to 75% domestically.</li><li>
Residence near a major U.S. airport hub.</li><li>
Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, PowerPoint, and general working knowledge of the Internet for business use.</li></ul> 
Preferred Qualifications<ul><li>
Experience supporting integrated delivery networks (IDNs), community oncology networks, or enterprise healthcare organizations.</li><li>
Experience working with Veterans Affairs (VA) and/or Department of Defense (DoD) healthcare systems.</li><li>
Experience leading Molecular Tumor Boards.</li><li>
Experience developing and executing enterprise scientific engagement strategies.</li><li>
Experience with molecular diagnostics, precision oncology implementation, or biomarker-driven clinical programs.</li></ul> 
Physical Demands<ul><li>
Ability to travel extensively by commercial airline and automobile.</li><li>
Ability to sit, stand, walk, and present for extended periods during customer meetings, conferences, and educational programs.</li><li>
Ability to transport presentation materials and equipment consistent with normal business travel requirements.</li><li>
Ability to use a computer and standard office equipment for extended periods.</li></ul> 
Training<ul><li>
All job-specific, safety, compliance, and regulatory training are assigned based on the job functions associated with this position.</li></ul> 
Other<ul><li>
This position requires up to 75% domestic travel.</li><li>
Candidates should reside near a major U.S. airport hub to facilitate frequent national travel.</li><li>
Position may require overnight travel, evenings, weekends, and holidays based on business needs, scientific meetings, customer engagements, and conferences.</li><li>
Participation in national scientific conferences, advisory boards, and enterprise customer meetings is expected.</li><li>
Additional responsibilities may be assigned to support evolving business and Medical Affairs priorities.</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

National Account Molecular Science Liaison

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary
 
The Senior Financial Analyst provides critical ongoing reporting and data insights to assist the CFO and the Executive Leadership team in making decisions about the Company&rsquo;s financial status and future. This position is located at the Irving, TX headquarters of Caris Life Sciences, directly reporting to the Finance Manager, and will work closely with the Finance and Accounting teams to produce accurate and timely reporting related to operations and the company&rsquo;s financial performance. The successful candidate will utilize strong business acumen, deep financial expertise and solid communication skills to become an effective partner at every level of the organization to understand business objectives and provide insightful reporting, decision support analysis, and forecasting in support of those objectives. 
Job Responsibilities
<ul><li>Serve as key support for forecasting, annual budget, long&ndash;term planning, monthly close, and analytics for a variety of functional groups.</li><li>
Develop, deploy, and communicate on-going monitoring of relevant business metrics, across financial and non-financial areas.</li><li>
Provide timely periodic and ad hoc financial reporting results to management team, analyze and communicate variances to plans, and provide performance improvement recommendations.</li><li>
Facilitate business planning efforts within assigned groups to ensure optimal implementation and on-going management of business models.</li><li>
Provide support for month-end close activities within established deadlines, including monthly reporting of production activities, department cost results and variance analysis, as well as any required journal entries.</li><li>
Identify, investigate, and resolve potential issues within tight time constraints.</li><li>
Load and maintain several data templates through Oracle/Hyperion, critical to monthly and periodic executive reporting.</li><li>
Perform industry analysis of competitors, trends and external benchmarking of key operating and financial metrics.
</li></ul>Required Qualifications
<ul><li>Bachelor&rsquo;s Degree in Business/Accounting/Finance required.</li><li>
2-4 years of experience in Corporate Finance and/or FP&amp;A functions.</li><li>
Experience with Oracle/EPBCS and Hyperion preferred.</li><li>
Direct experience in financial modeling, forecasting, and budgeting.</li><li>
Knowledge of the main components and drivers of income statement, balance sheet and statement of cash flows.</li><li>
Financial reporting skillsets to synthesize large amounts of data and information for presentation of resulting insights to business partners and executive leadership.</li><li>
Detail-oriented, excellent work ethic, positive attitude.</li><li>
Ability to manage multiple simultaneous projects effectively in a fast-paced, rapid-change, high-energy environment.</li><li>
Demonstrated results-driven orientation. Ability to self-manage and prioritize workload to meet delivery deadlines and solve complex problems.</li><li>
Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use.</li><li>
Strong verbal and written communication skills. Willingness to share and receive information and ideas from all levels of the organization in order to achieve the desired results.</li><li>
Commitment to the successful achievement of team and organizational goals through a desire to participate with and help other members of the team.</li></ul>
Preferred Qualifications
<ul><li>Advanced Excel skills (e.g., Power Query, PivotTables , macros) and PowerPoint.</li><li>
Familiarity with BI tools such as Tableau, Power BI, or Looker.</li><li>
Experience with Oracle EPBCS, Hyperion/Smart View, or similar tools.</li><li>
Experience with SQL or other data querying languages.</li><li>
Background in biotechnology, life sciences, or laboratory services.</li><li>
Exposure to private equity-backed environments or M&amp;A support.</li><li>
Understanding of healthcare reimbursement models or payer/provider dynamics.</li><li>
Experience automating reporting processes or building dashboards.</li></ul>
Physical Demands
<ul><li>Must possess ability to sit and/or stand for long periods of time.</li><li>
Must possess ability to perform repetitive motion.
</li></ul>Training
<ul><li>All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.</li></ul>
Other
<ul><li>At times may be required to work weekends/holidays.</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Senior Financial Analyst, Dallas, TX

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary
Lead and innovate as a Senior Staff Cloud DevOps Engineer specializing in AWS and Kubernetes to architect, implement, and optimize scalable, secure cloud-native infrastructure. Lead strategic initiatives, drive technical transformations, and provide expertise in cloud migrations, security implementations, and DevOps best practices. Develop and execute on long-term technical roadmaps, mentor junior engineers, and collaborate with executive leadership to align technology solutions with business objectives. Champion a culture of continuous improvement, knowledge sharing, and operational excellence across the organization.
Job Responsibilities<ul><li>
Architect and lead the implementation of large-scale, complex Kubernetes environments on AWS EKS, ensuring enterprise-grade availability, scalability, and security. Design and implement advanced features including multi-cluster management, service mesh architectures, and custom controllers.</li><li>
Drive strategic proof-of-concept (PoC) initiatives for emerging technologies, evaluating their potential impact on the organization's technical landscape and business goals.</li><li>
Lead the development of enterprise-wide standards for Kubernetes cluster lifecycle management, including upgrade strategies, security policies, and performance optimization frameworks.</li><li>
Provide expert-level consultation to cross-functional teams on cloud-native application design, microservices architecture, and container orchestration strategies.</li><li>
Architect and implement comprehensive, multi-layered observability solutions integrating metrics, logs, and traces. Develop predictive monitoring capabilities and establish organization-wide observability standards.</li><li>
Lead the adoption of advanced Infrastructure as Code (IaC) practices and oversee the implementation of sophisticated CI/CD and GitOps-based continuous delivery (e.g., ArgoCD) pipelines, including modular design patterns, reusable components, and automated testing frameworks for efficient application deployment and image management across multiple environments.</li><li>
Hands-on experience with GitOps-based continuous delivery using ArgoCD (app-of-apps, sync/health management, Helm/Kustomize deployments to Kubernetes).</li><li>
Develop and execute the organization's cloud security strategy, including the implementation of zero-trust architectures, automated compliance checks, and security-as-code practices. Translate complex regulatory and compliance requirements (e.g., HIPAA, SOC2, SOX) into actionable cloud implementation plans.</li><li>
Spearhead large-scale cloud migration and application modernization initiatives, collaborating with business stakeholders to align technical solutions with organizational objectives.</li><li>
Identify and implement strategic opportunities for process improvements and automation across the DevOps and cloud infrastructure landscape, developing and executing long-term roadmaps to drive continuous enhancement of cloud operations and DevOps practices.</li><li>
Lead critical incident response efforts and participate in on-call rotations to support and improve the reliability of critical cloud infrastructure.</li></ul>
Required Qualifications<ul><li>
Bachelor's degree in Computer Science, Information Technology, or related field.</li><li>
9+ years of experience in DevOps or Site Reliability Engineering roles.</li><li>
7+ years of hands-on experience with AWS services and cloud architecture.</li><li>
7+ years of hands-on experience with Kubernetes, including deep expertise in cluster management, troubleshooting, and optimization.</li><li>
Expert-level proficiency in at least one programming language (e.g., Python, Go) with a track record of developing and maintaining production-grade software.</li><li>
Extensive experience with Infrastructure as Code tools (e.g., Terraform, CloudFormation, AWS CDK) and ability to design scalable, modular IaC frameworks.</li><li>
Deep understanding of containerization technologies and orchestration platforms, including security best practices and performance optimization techniques.</li><li>
Proven experience in designing and implementing enterprise-grade CI/CD pipelines and DevOps workflows, preferred with GitLab CI, with hands-on GitLab CI/CD expertise (pipelines, runners, modular templates).</li><li>
Expert-level networking in complex AWS environments; hybrid/multi-cloud experience a plus.</li><li>
Strong analytical and problem-solving skills, with the ability to troubleshoot complex distributed systems and provide innovative solutions.</li><li>
Proven ability to lead PoC initiatives and evaluate new technologies.</li><li>
Demonstrated experience in creating and maintaining technical documentation and knowledge bases.</li><li>
Excellent communication skills, with the ability to effectively convey complex technical concepts to both technical and non-technical stakeholders, including executive leadership.</li><li>
Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use.</li><li>
Hands-on experience leveraging AI-assisted development tools (e.g., Claude, Cursor) to accelerate engineering work, including building automations, agents, and reusable skills/workflows that improve team productivity and reduce operational toil.</li><li>
Hands-on experience with GitOps-based continuous delivery using ArgoCD (app-of-apps, sync/health management, Helm/Kustomize deployments to Kubernetes).</li></ul>
Preferred Qualifications<ul><li>
AWS Professional level certifications (e.g., Solutions Architect Professional, DevOps Engineer Professional).</li><li>
Kubernetes certifications (e.g., CKA, CKAD, CKS).</li><li>
Experience with multiple cloud platforms (e.g., AWS, GCP) for multi-cloud architectures.</li><li>
Deep expertise in database technologies including design and optimization of distributed database systems including MySQL, PostgreSQL, and Serverless platforms.</li><li>
Proficiency with specific monitoring and observability tools such as DataDog and AWS CloudWatch.</li><li>
Hands-on experience with configuration management tools (e.g., Ansible, Chef, Puppet).</li><li>
Experience in implementing knowledge management systems or tools in a DevOps environment.</li><li>
Contributions to open-source projects or personal projects demonstrating cloud expertise.</li></ul>
Physical Demands<ul><li>
Ability to sit for extended periods while working on a computer.</li></ul>
Training<ul><li>
All job specific safety and compliance training are assigned based on the job functions associated with this employee.</li></ul>
Other<ul><li>
Job may require after-hours response to emergency issues and on-call availability as required</li></ul>
Annual Hiring Range
$170,000 - $220,000
Actual compensation offer to candidate may vary from posted hiring range based upon geographic location, work experience, education, and/or skill level. The pay ratio between base pay and target incentive (if applicable) will be finalized at offer. 
Description of Benefits<ul><li>
Highly competitive and inclusive medical, dental and vision coverage options</li><li>
Health Savings Account for medical expenses and dependent care expenses</li><li>
Flexible Spending Account to pay for certain out-of-pocket expenses</li><li>
Paid time off, including: vacation, sick time and holidays</li><li>
401k match and Financial Planning tools</li><li>
LTD and STD insurance coverages, as well as voluntary benefit options</li><li>
Employee Assistance Program</li><li>
Pet Insurance</li><li>
Legal Assistance</li><li>
Tuition Assistance</li></ul>
Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Senior Staff DevOps Engineer

<div>At Caris, we understand that cancer is an ugly word&mdash;a word no one wants to hear, but one that connects us all. That&rsquo;s why we&rsquo;re not just transforming cancer care&mdash;we&rsquo;re changing lives. 
We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: &ldquo;What would I do if this patient were my mom?&rdquo; That question drives everything we do. 
But our mission doesn&rsquo;t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare&mdash;driven by innovation, compassion, and purpose. 
Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.
Position Summary
The Clinical Data Coordinator is responsible for clinical data entry activities for the Caris Medical Affairs protocols and projects at the Caris Precision Oncology Alliance sites. The position will ensure the highest standards for clinical data integrity and quality are maintained in alignment with critical research efforts aimed to improve the treatment, health and medical outcomes for oncology patients. Responsible for the collection and review of clinical protocol research data; Interpretation of data (including appropriate source documentation) for entry into computerized databases; Good understanding of data definitions and case report forms and other information related to data collection for clinical research. Must respond to queries in a timely fashion. Schedule on-site visits to perform data review and EDC data entry.
Job Responsibilities
<ul><li>Abstract clinical data from subject source documentation.
</li><li>Enter clinical data into the study specific EDC case report forms.
</li><li>Clean the clinical data to verify accuracy.
</li><li>Update the EDC following verification of subject data, including the resolution of data queries.
</li><li>Track site goals and case report form completion.
</li><li>Prioritize site cases for analysis.
</li><li>Maintain study specific documentation.
</li><li>Perform QC audits of the clinical database.
</li><li>Support and adhere to Good Clinical Practices (GCP) guidelines, FDA, Institutional Review Board (IRB) and HIPAA regulations, Site Operating Procedures and ethical standards for the conduct of research clinical trials.
</li><li>Work closely with onsite team to confirm appropriate consenting is being performed and documented prior to data abstraction.
</li><li>Maintain to Caris and Site requirements for source document management and request for information.
</li><li>Act as site designated entry person.
</li><li>Willingness to travel to multiple investigative sites if required.
</li><li>Communicate effectively with the research team, investigator(s), Clinical Research Associate(s), study sponsor and ancillary staff.
</li></ul>Required Qualifications
<ul><li>Position requires 3-5 years of experience in data collection activities within a GCP/clinical research regulatory environment.
</li><li>Knowledgeable in critical elements for success in clinical trials. GCPs, ICH, and Code of Federal Regulations.
</li><li>Clinical study experience in the field of Oncology.
</li><li>Strong medical terminology understanding.
</li><li>Experience in both small and large scale project planning and reporting with strong communication and presentation skills.
</li><li>Experience in providing training for both internal and external staff with a mentorship approach for less experienced colleagues.
</li><li>Experience with EDC systems.
</li><li>Proficient in Microsoft Office Suite, specifically Word, Excel, Outlook, and general working knowledge of Internet for business use .
</li></ul>Physical Demands
<ul><li>Must possess ability to sit and/or stand for long periods of time.
</li></ul>Training
<ul><li>All job specific, safety, and compliance training are assigned based on the job functions associated with this employee.
</li></ul>Other
<ul><li>This position may require occasional evenings and overtime.
</li></ul>Conditions of Employment: Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions ) and reference verification.
This job description reflects management&rsquo;s assignment of essential functions. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.</div>

Clinical Data Coordinator I

Join Caris Life Sciences and explore 7   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.