Jobs at Tempus
37,634 open positions
Senior Biostatistician, Medical Affairs
Company: Tempus
Location: Boston, MA
Posted Aug 08, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Top candidates will also have experience working with clinical and research data pipelines, and/or doing biostatistical, epidemiological, or HEOR research on observational healthcare data.Responsibilities:Collaborate on clinical projects with external academic partnersCollaborate with internal and external stakeholders in the design, analysis, and interpretation of clinical real-world studiesProvide clients with guidance on Tempus data model and perform data support, including but not limited to: answer collaborators’ questions, perform data quality control, select and profile cohortsCommunicate results and scientific findings on a regular basis, using appropriate communication and visualization tools commonly used for biological researchStay current with the latest methodological advances in real-world studiesThis position has the potential to publish abstracts and manuscripts and participate in poster presentations in collaboration with external partnersRequired Experience:Advanced degree (Master’s or PhD) in Computational Biology, Biostatistics/Statistical Genetics, Bioinformatics, Biomedical Informatics, Biometrics, Data Science for Health or similar with 2+ years of experience working with clinical dataBiological or medical knowledge e.g., Human Disease, Genetics/Genomics, Molecular Biology, or ImmunologyStrong proficiency in R or Python and/or other programming languagesProficiency with statistical modeling methods, including time-to-event analysis (TTE), and methodology expertise with observational datasets preferredStrong project management skills: defining research questions, writing scientific roadmaps, tracking progress against those roadmaps, aligning scientific results with business outcomesStrong communication and presentation skillsAble to effectively present research results to study team and other collaborators, including results interpretation and drawing appropriate inferences based on study design/statistical methods as well as assessment of study limitationsCommunicating technical concepts to non-technical audiencesCollaborative mindset, an eagerness to learn and a high-integrity work ethicExperience providing mentorship and/or management to junior colleaguesSharp attention to detail and passion for delivering high-quality and timely analytics deliverablesNice to have:Experience in the design and analysis of clinical studies or real-world data studiesFamiliarity with SQLExperience in cancer genetics, immunology, or molecular biologyExperience in extracting meaningful insights from genomics data (RNA/DNA-seq)Experience with biomarker identification and characterizationClient-facing or consulting experience and comfort with presenting results to stakeholdersExperience doing inferential statistics on observational dataExperience putting data science workflows into productionExperience with version control, software testing, GCP technical stackUnderstanding of cancer genomicsLI-GL1LI-HybridLI-RemoteWe are an equal opportunity employer. We work directly with the Tempus Medical Sciences Team and oncology research leaders to understand their goals and translate their scientific questions into exploratory data analyses.We are seeking a highly motivated, capable Senior Biostatistician of Medical Affairs with experience and interest in oncology and/or molecular data. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.With the advent of genomic sequencing, digital imaging, and techniques for large-scale clinical data processing, we have powerful new weapons in the data-driven fight against cancer. We’re on a mission to connect an entire ecosystem to redefine how genomic and clinical data is used for evidence-based medicine.On Tempus’ Real World Data Analytics (RWDA) team, we work with Key Opinion Leaders in academia and the research community to generate novel insights with real-world data. Passionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way.
Translational Scientist
Company: Tempus
Location: Remote
Posted Aug 04, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. in Computational Biology, Bioengineering, Cancer Biology or Molecular BiologyMinimum 5+ years in drug development leveraging genomic and multimodal data for drug discovery and development Strong understanding of molecular data and artificial intelligence in drug discoveryPrior Consulting and/or client facing experience is highly desirableLI-BL1We are an equal opportunity employer. Our Translational Scientists are comfortable on a whiteboard designing studies or a board room with an Executive, providing trusted technical advice for our partners and clients. This candidate will be responsible for cultivating and growing Tempus partnerships with pharmaceutical and biotechnology clients to support them in advancing their research, clinical and/or commercial programs. The Tempus precision medicine platform brings multiple capabilities together such as Multimodal Datasets, Artificial Intelligence applications, Sequencing and Clinical Trial recruitment services to change the future of drug development. ResponsibilitiesDevelop and Drive global account strategy in coordination with the account teamBecome an expert in the partner’s strategy, pipeline and portfolio to proactively determine all areas that the Tempus platform could be leveraged for advancing innovationBuild and maintain R&D relationships as the trusted technical advisorWork directly with clients to Co-architect solutions and projects that leverage the Tempus platform to solve customers' challenges. Partner with our clients to develop and announce impactful case studies leveraging the Tempus platform to advance precision medicineAuthor whitepapers and create demonstrations illustrating the value of multimodal analysis and AI in drug discovery in coordination with our Research, Engineering & Data Science teamsDevelop the educational material necessary to onboard our clients onto multimodal analysis using Tempus data and platformContribute to the development of the Life Sciences portfolio by providing feedback to Leadership regarding client responses and suggestions; maintain a solution-oriented mindset Track progress against defined strategic objectives and goals; review progress/setbacks frequently with broader Account Team and Tempus LeadershipTravel approximately 40% of working time, domestically and internationallyOther duties as assignedQualificationsProven track record of developing solutions utilizing molecular and multimodal dataProven history of establishing credibility as a trusted advisor Demonstrated ability to influence without authority (both with internal and external stakeholders)Strong understanding of Molecular, Clinical Trial and Real World Evidence Platforms Learning agility to adapt to a rapidly changing environment Proactive mindset that bridges ideas to implementable solutions, and can help move both internal and external stakeholders to quickly solve problemsExperiencePh.D. Our data empowers researchers to better characterize and understand disease, and to drive better outcomes through precise, individualized care.We built Tempus to collect, structure, and organize data from disparate data silos into a comprehensive dataset to accelerate the pace of innovation and discovery in healthcare. This role will focus on collaborating with the world’s leading biopharmaceutical organizations utilizing the Tempus platform to enable multimodal analysis and Artificial Intelligence across the entire drug development lifecycle. With the expansion of multi-modal healthcare data and recent advancements in AI, that’s about to fundamentally change. Tempus is a healthcare technology company at the forefront of that change to leverage data to improve patient lives.Tempus' proprietary platform connects an entire ecosystem of real-world data to deliver real-time, actionable insights to physicians. And now we are looking for a Translational Scientist to join our rapidly growing Life Sciences team. Passionate about making a difference in the world of cancer genomics?With the advent of genomic sequencing, we can finally decode and process our genetic makeup; however, computer technology has had limited impact in healthcare.
Senior Software Engineer, Developer Tools
Company: Tempus
Location: New York City, NY
Posted Aug 08, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits, depending on the position.California Pay Range$130,000—$175,000 USDWe are an equal opportunity employer. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits, depending on the position.New York Pay Range$130,000—$175,000 USDThe expected salary range below is applicable if the role is performed from [California] and may vary for other locations. Author clear and concise documentation to reduce support costs Minimum Qualifications:Bachelor’s degree (or higher) in Computer Science, Software Engineering, or Data Science5+ years of professional experience as a software engineer OR a minimum of three years with an advanced degree3+ years of command-line experience in macOS or Linux1+ year of recent coding experience in Golang1+ year of experience with Postgres or MySQLCoding experience in PythonHands on experience with Google Cloud Platform, Amazon Web Services, or AzureOutstanding written and verbal communication skillsBonus Points for:Prior experience building developer tools, plug-ins for developer tools, linters, etc.Experience as a full stack developerCoding experience in TypeScriptGCP certification(s)Node.jsPrior exposure to Concourse, Jira, Confluence, GitHubDeep knowledge of test automation, CI/CD, DevOps, QA, or ScrumReact.jsTerraformKnowledge of HIPAA, HITRUST, or ISOCoding experience in RustLI-SH1LI-HybridLI-OnsiteThe expected salary range below is applicable if the role is performed from [New York] and may vary for other locations. We’re looking to expand into more interesting tooling areas such as VS Code plug-ins to help our Product, Compliance, Quality Solutions, and Operations partners. By optimizing the developer experience, we’re able to help Tempus deliver the right experience to our physicians and drive positive outcomes for our patients, faster. Our team’s existing portfolio spans from brew-like CLI tools to full-stack applications bearing resemblances to TinyURL. Join us in our mission to help delight our fellow engineers.What You Will Do:Be a thought leader and key contributor within the Developer Tools teamRelentlessly partner with teams company-wide to identify pain points in their development processesIndependently design and implement thoughtful features and tools to improve software engineering productivity and code qualityMentor junior peers and contribute to the success of teammates via code reviews, to ensure adherence to industry best practicesRegularly provide support to internal customers and create/deliver training sessions. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.Are you passionate about developer tooling?The Developer Tools team creates internal tools and frameworks focused on improving the lives of every software engineer working at the company. Passionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way.
Senior Biostatistician, Medical Affairs
Company: Tempus
Location: Peninsula
Posted Aug 08, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Top candidates will also have experience working with clinical and research data pipelines, and/or doing biostatistical, epidemiological, or HEOR research on observational healthcare data.Responsibilities:Collaborate on clinical projects with external academic partnersCollaborate with internal and external stakeholders in the design, analysis, and interpretation of clinical real-world studiesProvide clients with guidance on Tempus data model and perform data support, including but not limited to: answer collaborators’ questions, perform data quality control, select and profile cohortsCommunicate results and scientific findings on a regular basis, using appropriate communication and visualization tools commonly used for biological researchStay current with the latest methodological advances in real-world studiesThis position has the potential to publish abstracts and manuscripts and participate in poster presentations in collaboration with external partnersRequired Experience:Advanced degree (Master’s or PhD) in Computational Biology, Biostatistics/Statistical Genetics, Bioinformatics, Biomedical Informatics, Biometrics, Data Science for Health or similar with 2+ years of experience working with clinical dataBiological or medical knowledge e.g., Human Disease, Genetics/Genomics, Molecular Biology, or ImmunologyStrong proficiency in R or Python and/or other programming languagesProficiency with statistical modeling methods, including time-to-event analysis (TTE), and methodology expertise with observational datasets preferredStrong project management skills: defining research questions, writing scientific roadmaps, tracking progress against those roadmaps, aligning scientific results with business outcomesStrong communication and presentation skillsAble to effectively present research results to study team and other collaborators, including results interpretation and drawing appropriate inferences based on study design/statistical methods as well as assessment of study limitationsCommunicating technical concepts to non-technical audiencesCollaborative mindset, an eagerness to learn and a high-integrity work ethicExperience providing mentorship and/or management to junior colleaguesSharp attention to detail and passion for delivering high-quality and timely analytics deliverablesNice to have:Experience in the design and analysis of clinical studies or real-world data studiesFamiliarity with SQLExperience in cancer genetics, immunology, or molecular biologyExperience in extracting meaningful insights from genomics data (RNA/DNA-seq)Experience with biomarker identification and characterizationClient-facing or consulting experience and comfort with presenting results to stakeholdersExperience doing inferential statistics on observational dataExperience putting data science workflows into productionExperience with version control, software testing, GCP technical stackUnderstanding of cancer genomicsLI-GL1LI-HybridLI-RemoteWe are an equal opportunity employer. We work directly with the Tempus Medical Sciences Team and oncology research leaders to understand their goals and translate their scientific questions into exploratory data analyses.We are seeking a highly motivated, capable Senior Biostatistician of Medical Affairs with experience and interest in oncology and/or molecular data. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.With the advent of genomic sequencing, digital imaging, and techniques for large-scale clinical data processing, we have powerful new weapons in the data-driven fight against cancer. We’re on a mission to connect an entire ecosystem to redefine how genomic and clinical data is used for evidence-based medicine.On Tempus’ Real World Data Analytics (RWDA) team, we work with Key Opinion Leaders in academia and the research community to generate novel insights with real-world data. Passionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way.
Senior Software Test Engineer, Customer Systems
Company: Tempus
Location: Chicago, IL
Posted Aug 02, 2023
The text is about Tempus, a company that uses AI to impact clinical care in a meaningful way. They are looking for Quality Engineers to work on delivering actionable insights to customers via web and mobile solutions. The candidate will work closely with the product development team and become the subject matter expert on the system's behavior and customer needs. They will develop a test strategy, improve existing practices, and drive changes. The candidate should have a Bachelor's degree in Computer Science, 5+ years of experience in coding and test methodologies, and experience in the complete software development life cycle. They should have prior experience with Continuous Integration tooling, Docker, Infrastructure-as-a-Service, Service Oriented Architecture, and coding with Typescript/Javascript. The company is an equal opportunity employer.
Senior Biostatistician, Medical Affairs
Company: Tempus
Location: Chicago, IL
Posted Aug 08, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Top candidates will also have experience working with clinical and research data pipelines, and/or doing biostatistical, epidemiological, or HEOR research on observational healthcare data.Responsibilities:Collaborate on clinical projects with external academic partnersCollaborate with internal and external stakeholders in the design, analysis, and interpretation of clinical real-world studiesProvide clients with guidance on Tempus data model and perform data support, including but not limited to: answer collaborators’ questions, perform data quality control, select and profile cohortsCommunicate results and scientific findings on a regular basis, using appropriate communication and visualization tools commonly used for biological researchStay current with the latest methodological advances in real-world studiesThis position has the potential to publish abstracts and manuscripts and participate in poster presentations in collaboration with external partnersRequired Experience:Advanced degree (Master’s or PhD) in Computational Biology, Biostatistics/Statistical Genetics, Bioinformatics, Biomedical Informatics, Biometrics, Data Science for Health or similar with 2+ years of experience working with clinical dataBiological or medical knowledge e.g., Human Disease, Genetics/Genomics, Molecular Biology, or ImmunologyStrong proficiency in R or Python and/or other programming languagesProficiency with statistical modeling methods, including time-to-event analysis (TTE), and methodology expertise with observational datasets preferredStrong project management skills: defining research questions, writing scientific roadmaps, tracking progress against those roadmaps, aligning scientific results with business outcomesStrong communication and presentation skillsAble to effectively present research results to study team and other collaborators, including results interpretation and drawing appropriate inferences based on study design/statistical methods as well as assessment of study limitationsCommunicating technical concepts to non-technical audiencesCollaborative mindset, an eagerness to learn and a high-integrity work ethicExperience providing mentorship and/or management to junior colleaguesSharp attention to detail and passion for delivering high-quality and timely analytics deliverablesNice to have:Experience in the design and analysis of clinical studies or real-world data studiesFamiliarity with SQLExperience in cancer genetics, immunology, or molecular biologyExperience in extracting meaningful insights from genomics data (RNA/DNA-seq)Experience with biomarker identification and characterizationClient-facing or consulting experience and comfort with presenting results to stakeholdersExperience doing inferential statistics on observational dataExperience putting data science workflows into productionExperience with version control, software testing, GCP technical stackUnderstanding of cancer genomicsLI-GL1LI-HybridLI-RemoteWe are an equal opportunity employer. We work directly with the Tempus Medical Sciences Team and oncology research leaders to understand their goals and translate their scientific questions into exploratory data analyses.We are seeking a highly motivated, capable Senior Biostatistician of Medical Affairs with experience and interest in oncology and/or molecular data. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.With the advent of genomic sequencing, digital imaging, and techniques for large-scale clinical data processing, we have powerful new weapons in the data-driven fight against cancer. We’re on a mission to connect an entire ecosystem to redefine how genomic and clinical data is used for evidence-based medicine.On Tempus’ Real World Data Analytics (RWDA) team, we work with Key Opinion Leaders in academia and the research community to generate novel insights with real-world data. Passionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way.
QA Document Control Manager
Company: Tempus
Location: Chicago, IL
Posted Aug 06, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits, depending on the position.California Pay Range$110,000—$150,000 USDWe are an equal opportunity employer. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits, depending on the position.New York Pay Range$110,000—$150,000 USDThe expected salary range below is applicable if the role is performed from [California] and may vary for other locations. Actual salary may vary based on qualifications and experience. Manager, Quality Assurance and will play a key technical leadership role for the software test organization. Responsibilities:Manage and administer electronic Document Management System across sites and acquisitions to ensure compliance to applicable internal procedures, global regulatory requirements, and standards.Support update, review and approval of controlled documents, including procedures, work instructions, protocols, templates and technical documents.Become extremely well-versed in the electronic Document Management system and create company training materials in a timely manner.Implement Document Management solutions with a primary focus on Document Control and records management.Track, trend, and monitor metrics related to Document Management and Control, providing reports as necessary.Drives continuous improvement to support a sustainable framework for QMS document control activities to enable simplification and standardization.Collaborate with cross-functional partners to develop usable and compliant procedures, serving as a subject matter expert in regulatory compliance audits and inspections.Lead and drive audit actions and CAPA’s associated with the Document Management and Control.Ensure Document Controls are in compliance with CAP/CLIA and FDA regulations, as well as ISO and other regulatory standards.Collaborate with cross-functional partners such as Lab Operations, R&D, Regulatory, Medical Affairs, etc. to seek their input into the development of procedures, understanding the support they need and addressing their concerns and issues.Strategize on building efficiencies within Document Management and Controls. Oversee, mentor, and develop staff.Other duties and projects, as assignedRequired Education & Experience:Requires a Bachelor's degree or equivalent related experience, 10+ years of experience in a documentation-related position in a regulated environment, and 5+ years of supervisory experienceStrong written and oral communication skills, attention to detail, and the ability to prioritize and organize a busy workload are also requiredStrong stakeholder management and ability to influence othersAbility to lead and collaborate with a diverse team (entry level to seasoned) through growth and change, including internal and external challengesExperience with different electronic document management systemsIntermediate to advanced working knowledge of medical device regulations and standards (ISO 13485:2016, FDA QSR)Intermediate computer skills and software applications, including experience with Microsoft Office tools (Outlook, Word, Excel, PowerPoint)Proven experience in working in a cross-functional team environment as well as the ability to function independentlyAbility to be open-minded, define and create solutions to challenges or opportunitiesAbility to communicate with all levels of technical and operations personnelAbility to gather and organize informationAbility to create processes and workflowsAbility to handle a variety of projects at the same timeProven ability to prioritize and organize a busy and changing workloadProven ability to manage assigned projects with little supervisionLI-SH1LI-HybridThe expected salary range below is applicable if the role is performed from [New York] and may vary for other locations. This position ensures that the Document Controls processes are in compliance with CAP/CLIA, FDA regulations, ISO and other regulatory standards. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.As Document Control Manager, you will lead the development, effective implementation, and continuous improvement of Document Management and Controls across multiple sites and business acquisitions. You will report to the Sr. Passionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way.
Supply Chain Data Analyst
Company: Tempus
Location: Chicago, IL
Posted Aug 11, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.Duties and Responsibilities:Develop firm understanding of systems and processes utilized across supply chain, lab, and lab support teamsLead process improvement and reporting on existing toolsDevelop and maintain new reporting dashboardsLead development of new integrated and automated data tools Work cross functionally with lab support teams to fully understand downstream effects of systems and data changesWrite and review SOP/work instruction for new data processesReport, Automate, Improve, and Develop processes including:System implementation and data mappingShipping centralization project development and oversightAudits on monthly transactions and expendituresDaily, Weekly, and Monthly reporting packsLooker DashboardsNetsuite Saved SearchesAssist with other supply chain vertical data needs as capacity allows.Preferred Qualifications:Bachelor’s Degree in a related field Minimum 3 years relevant experienceDemonstrable experience in Netsuite or major ERP queryingDemonstrable experience in Looker, Mode, Tableau or similar data queryingHighly organized and systematic, superb attention to detail and ability to complete tasks with a high degree of accuracyExcellent communication skillsProven initiative and ability to work as part of a high-level team while working independently on mission-critical tasksProven ability to learn new skills quickly and adapt to new processes smoothly We are an equal opportunity employer. Passionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way.
Machine Learning Scientist, Generative AI
Company: Tempus
Location: Chicago, IL
Posted Aug 13, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Attend relevant conferences, workshops, and seminars. Experience with healthcare-specific frameworks (e.g., DICOM, FHIR) is a plus.Solid knowledge of machine learning concepts, including deep learning, optimization algorithms, regularization techniques, and modelBias-to-action, appetite for high-risk high-gain projects with a pragmatic approach to rapid and measurable progressStrong track record in publications, patents, and/or launched products in this spaceNice-to-haves:Experience working with sensitive healthcare data, medical imaging modalities, clinical workflows, and healthcare terminology. A strong academic background with a focus on generative AI and healthcare applications is highly preferred.Extensive experience in developing and implementing generative AI models, such as GANs, VAEs, and related architectures.Proficiency in programming languages commonly used in AI research, such as Python and TensorFlow/PyTorch. Collaborate with academic and industry partners to advance the state-of-the-art in generative AI for healthcare.Qualifications:Ph.D. or Master's degree in Computer Science, Artificial Intelligence, Biomedical Engineering, or a related field. Work closely with engineering teams to integrate your models into healthcare platforms, systems, or applications. Familiarity with electronic health records (EHRs) and medical imaging formats (e.g., DICOM) is advantageous.Experience in late-stage startup environmentExperience building and bringing practical use, knowledge graphs and graph-based machine learning modelsExpertise with embedding, multimodal fusionLI-EV1We are an equal opportunity employer. Collaborate with domain experts, clinicians, and researchers to validate and refine the models' outputs.Collaborative Teamwork: Collaborate closely with cross-functional teams, including healthcare professionals, data scientists, software engineers, and product managers. Ensure scalability, efficiency, and robustness of the deployed solutions.Regulatory Compliance and Ethical Considerations: Stay up to date with healthcare regulations, privacy laws, and ethical considerations relevant to the development and deployment of AI in healthcare. Ensure compliance with HIPAA, GDPR, and other applicable standards throughout the development process.Continuous Learning and Industry Engagement: Stay actively involved in the healthcare and AI research communities.
QA Document Control Specialist
Company: Tempus
Location: Chicago, IL
Posted Aug 08, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. to seek ensure timely document reviews and approvalsSupport leadership on building efficiencies within Document Management and Controls.Other duties and projects, as assignedRequired Education & Experience:Requires a Bachelor's degree or equivalent related experience, 2+ years of experiencein a documentation-related position in a regulated environmentStrong written and oral communication skills, attention to detail, and organizedExperience with working in an electronic document management systemsExperience working in a medical device, clinical laboratory, or other regulated environment.Intermediate computer skills and software applications, including experience with Microsoft Office tools (Outlook, Word, Excel, PowerPoint) or Google Suite applicationsProven experience in working in a cross-functional team environment as well as the ability to function independentlyAbility to be open-minded, define and create solutions to challenges or opportunitiesAbility to communicate with all levels of technical and operations personnelAbility to gather and organize informationAbility to create processes and workflowsLI-SH1LI-HybridWe are an equal opportunity employer. You willreport to the Document Control Manager and will play a key role in ensuring document controlcompliance to applicable global regulations and standards.Responsibilities:Support the administration of the electronic Document Management System across sitesand acquisitions to ensure compliance to applicable internal procedures, globalregulatory requirements, and standards.Support update, review and approval of controlled documents, including procedures,work instructions, protocols, templates and technical documents.Become extremely well-versed in the electronic Document Management system tofacilitate compliant reviews and approvalsSupport implementation Document Management solutions with a primary focus onDocument Control and records management.Support quality metrics related to Document Management and Control, providing reportsas necessary.Support continuous improvement to support a sustainable framework for QMS documentcontrol activities to enable simplification and standardization.Collaborate with cross-functional partners to develop usable and compliant procedures,serving as a subject matter expert in regulatory compliance audits and inspections.Support audit actions and CAPA’s associated with the Document Management andControl.Support Document Controls compliance with CAP/CLIA and FDA regulations, as well asISO and other regulatory standards.Collaborate with cross-functional partners such as Lab Operations, R&D, Regulatory,Medical Affairs, etc. This position ensures that the Document Controls processes are incompliance with CAP/CLIA, FDA regulations, ISO and other regulatory standards. Tempus' proprietary platform connects an entire ecosystem ofreal-world evidence to deliver real-time, actionable insights to physicians, providing criticalinformation about the right treatments for the right patients, at the right time.As Document Control Specialist, you will support the development, effective implementation,and continuous improvement of Document Management and Controls across multiple sites andbusiness acquisitions. Passionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impactclinical care in a meaningful way.
Product Manager
Company: Tempus
Location: Chicago, IL
Posted Aug 03, 2023
The text is about Tempus, a company developing AI to impact clinical care in the healthcare industry. The company is looking for a Product Manager to work on cutting-edge software solutions for cancer care. The role involves working with various teams, conducting product analysis, and communicating with users.
Life Sciences Marketing Associate
Company: Tempus
Location: Chicago, IL
Posted Aug 05, 2023
We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. The Marketing Associate will help execute on our marketing strategy and collaborate with different functional groups (Life Sciences Sales Teams, Medical Affairs, Legal, R&D, and Regulatory) to help support our Life Sciences function in various campaigns and projects. How You’ll ContributeResponsible for creating wow-factor marketing campaigns throughout various channels, including email, web, social, etcSupport sales throughout a wide range of initiatives, like creating sales enablement tools, identifying success stories, etc.Responsible for the legal, regulatory, and medical approval process for all external facing marketing materials.Point person for reporting out on campaign KPIs, website analytics, campaign execution, webinars, and help direct the Marketing team to opportunities that are most important for success, based on the metrics we have available. Lead all marketing programs for key conferencesPreferred Qualifications2+ years of marketing experience preferredStrong organization skills with ability to work on multiple projects simultaneouslyAbility to collaborate with cross functional teams and solve problems quickly Resourceful and flexible Responds to changes quickly and thoughtfullyStrong excel skills preferredSalesforce experience preferredGoogle Analytics proficiency preferred College degree requiredLI-EH1We are an equal opportunity employer. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.We’re looking for a high performing and motivated individual to join our Life Sciences marketing team as a Marketing Associate. Passionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way.