Jobs at Tempus
37,634 open positions
Senior Associate, Site Contracts and Budgets
Company: Tempus
Location: Chicago, IL
Posted Aug 21, 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. Manager, Site Contracts.Review contracts and other documents for completeness and accuracy.May support additional site start-up tasks, where necessary.Performs other duties as assigned.May involve travel (rare).Demonstration of Values:Consistently strives to demonstrate the following values:Recognizes that the team is always stronger than the individual. Seeks to inspire others by demonstrating consistently strong performance. Treats people with respect regardless of role or point of view. Listens well and seek to understand before reacting.Provides candid, helpful and timely feedback to colleagues. Demonstrates curiosity about and contributes effectively to areas outside of their specialty. Keeps the bigger picture in mind when making decisions. Never stops learning. Questions assumptions and offers suggestions for improvement. Focuses on results rather than process and seeks to minimize complexity when process is required.Identifies and addresses root causes, not symptoms. Demonstrates poise in stressful situations. Strives to always do the right thing. Questions actions that are incongruent with Tempus Compass values.&8239; Minimum Qualifications:High school/secondary level education required. Minimum of 2 years of experience with budgeting and contracting process.Effective communication and interpersonal skills.Excellent organizational skills, attention to detail and ability to handle multiple competing and changing priorities within tight timelines.Able to proactively anticipate needs and follow through on all assigned tasks. Proficient in Microsoft Word and Excel, and in Adobe Acrobat. Preferred Qualifications: Bachelor’s degree preferred. 2 or more years of previous related CRO or Pharma experience highly preferred.LI-SH1 LI-RemoteWe are an equal opportunity employer. Will work cross-functionally to ensure timely distribution of assigned contracts. Job Responsibilities:Serve as the primary contact negotiator for all study related contract activities to meet the business objectives.Is responsible for negotiating, tracking, and finalizing the Confidentiality Agreements (CDA), Clinical Trial Agreements (CTA), budgets as well as amendments to these documents, as needed.Maintains tracking (CTMS) regarding site contracts and budgets and provides regular updates to the project team and client regarding status and efforts to ensure timelines are maintained. Proactively communicates updates on contract and budget status and workflow progress to Sr. Manager and other internal stakeholders and teams.Attends internal team meetings as necessary to report on status and to ensure alignment on the strategy of execution and risk management for completion of study budgets and contracts (and amendments) to meet study timelines and goals. Collaborates with Manager/Senior Manager, Regulatory Operations to ensure efficiency and appropriate prioritization of sites.Escalates any difficulties with negotiation, all site and Client concerns and any potential risks to the Sr. 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.Summary:Provides support for site contract and budget activities for all assigned projects in accordance with applicable regulatory guidelines/requirements, Tempus Compass Standard Operating Procedures (SOPs) and project specific plans. Will be the point of contact with outside parties on contract and budget matters. 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.
Regulatory Submissions Specialist
Company: Tempus
Location: Chicago, IL
Posted Aug 17, 2023
Tempus, a company specializing in precision medicine, is seeking a Regulatory Submissions Specialist. The role involves conducting research, preparing and submitting documents to regulatory authorities, managing document writing and review processes, and collaborating with interdisciplinary teams. The ideal candidate should have a degree in biomedical/life sciences, at least 3+ years of Regulatory Affairs experience, and strong organizational and problem-solving skills. Preferred qualifications include FDA experience, knowledge of genomics, bioinformatics, and healthcare technology.
Senior Product Manager, Data Governance
Company: Tempus
Location: Peninsula
Posted Aug 18, 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$120,000—$170,000 USDWe are an equal opportunity employer. )Ability and interest to quickly ramp up on new concepts in the fields of genomics, oncology, etcExcellent written and verbal communication skills, including the ability to act as translator among diverse teams of biologists, medical professionals, engineers, operators, and data scientists. Experience in complex data systems, data de-identification, data modeling, healthcare informatics and/or AI-driven data enrichmentLI-SH1The expected salary range below is applicable if the role is performed from [New York] and may vary for other locations. 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$120,000—$170,000 USDThe expected salary range below is applicable if the role is performed from [California] and may vary for other locations. And, it will inform the roadmap for infrastructure and documentation developed by our Real World Data team such that producers and consumers can more easily create, maintain, and analyze data. Actual salary may vary based on qualifications and experience. You’ll also partner with engineering leaders on inputs that inform the infrastructure and standards that will allow for increased data security and compliance.What You'll Do:Immerse yourself in the tough problems we’re solving and partner with scientists, engineers, and designers to develop elegant software solutions to solve those problemsBroadly lead our Data De-Identification programs, owning everything from the end-to-end data de-identification strategy to the roadmap for addressing critical third party reviews and attestation.Turn Voice of Customer feedback from our data customers into a high-impact strategy and plan for data usability improvements.Conduct deep product analysis and use the data to guide the short- and long-term roadmap for the Data de-identification engineering team.Own stakeholder communication and expectation management around roadmap and delivery timelines for your products, in particular to senior legal, application security and engineering operations stakeholders.Build the expert de-ID roadmap across Tempus data productsAssess security risk posed by increased data use across sources and support rollout of mitigation initiatives.Enable overall data governance and lineage strategy that aligns with business goalsQualifications:5+ years of technical experience in product management or in building software in the tech or healthcare industryExceptional ability to build and drive product strategy cross-functionally, across teams whose roadmaps you manage directly and those you don’tAbility to manage several programs at once and work proactively to align multi-disciplinary stakeholders.A history of building and using product analytics to drive clear decisionsExperience with software development and project management tools (JIRA, Trello, etc. In this role, you will be a critical leader in developing one of the most novel and useful data assets in the AI and precision medicine space today.You will develop a central data de-identification strategy focused on minimally necessary PHI data use, data auditability and usage monitoring, and lead cross functional initiatives to ensure that we not only have the largest, but also the most secure collection of data. The strategy you build will yield measurable improvements to the work being done by our data customers. These data are used both internally for development of models and diagnostics, and externally by Life Sciences partners and others.
Program Manager, CDx
Company: Tempus
Location: Chicago, IL
Posted Aug 18, 2023
Tempus is seeking a CDx Program Manager to oversee sequencing and companion diagnostic projects, manage day-to-day operations, and collaborate with various internal teams. The ideal candidate should have a bachelor's degree, 5+ years of relevant experience, strong attention to detail, and excellent presentation skills. Prior work in life sciences, genomic sequencing, or oncology is a plus.
Principal Software Quality Engineer
Company: Tempus
Location: Chicago, IL
Posted Aug 22, 2023
The text discusses the role of AI in clinical care, specifically at Tempus. They are looking for a Principal Software Validation Engineer to ensure compliance to GxP computer system validation and author related documentation. The candidate should have experience in FDA regulated domains, Computer System Validation, and FDA 21 CFR Part 11. They also require knowledge of quality system principles, project management skills, and experience with SDLC tools.
Quality Control Technologist I-IV
Company: Tempus
Location: Chicago, IL
Posted Aug 24, 2023
The job posting is for a Quality Control Technologist at Tempus, a company that connects an ecosystem of real-world evidence to deliver real-time insights to physicians. The role involves maintaining equipment and reagent compliance, creating new equipment functionality, and providing quality control support in a high-volume clinical molecular laboratory.
Biostatistician, Medical Affairs
Company: Tempus
Location: Chicago, IL
Posted Aug 21, 2023
The text discusses the use of AI and real-world data analytics in precision medicine, with a focus on cancer research. The position requires experience with clinical data, statistical modeling, and project management. The company values diversity and equality.
Real World Data Scientist, RWDA
Company: Tempus
Location: San Francisco, CA
Posted Aug 18, 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 RWD scientist will then perform sample size and power calculations, execute interim and final statistical analyses, communicate the findings to the stakeholders, and prepare written reportsWork on complex problems, exercising judgment in selecting and adapting methods as appropriateWork in interdisciplinary groups of scientists, engineers, and product developers to translate research into clinically actionable insights for our clientsStay current with the latest methodological advances in real world studiesComply with all applicable regulations and Company proceduresRequired Experience:1+ years of post-grad experience in data science, bioinformatics, biostatistics, epidemiology, immunology, public health, or related fields. Computational skills using Python, R or SAS, especially relevant statistical tools and packagesIdeal candidates will possess:Proficient in SQLStrong data manipulation and analysis skills Ability to tackle large, ambiguous problems Strong communication and presentation skillsSelf-starterExtensive experience with time to event analysis and methodologyFamiliarity with machine learning techniques and the advantages and disadvantages of different approaches, especially with respect to predictive and prognostic algorithms in medical researchExperience in cancer genetics, immunology, or molecular biologySelf-driven and works well in interdisciplinary teamsCollaborative mindset, an eagerness to learn and a high integrity work ethicSharp attention to detail and passion for delivering high quality and timely analytics deliverablesAble 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 limitationsNice to have:Experience with version control and software testingExperience working in oncology Phase II-IV clinical trials and/or experience with the analysis of RWD studies (e.g. using claims, EHR or registry data sources)Hands-on experience in helping to prepare regulatory submissions to the FDAExperience supporting data science teams in model building and validationClient facing or consulting experience and comfort with presenting results to stakeholdersLI-GL1We are an equal opportunity employer. We are seeking a highly motivated and capable Real World Data Scientist with extensive experience and interest in design and analysis of pharmacoepidemiological studies to join our team.Responsibilities:Participate in clinical projects with external Pharma, academic and other partnersRepresent the Real World Data function and collaborate with internal and external stakeholders in the design, analysis, interpretation and publication of clinical real world studiesContribute to study protocols and statistical analysis plans. 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.The Real World Data Analytics team at Tempus partners with external Pharma, biotech and academic institutions to provide best in class data, analysis and methodological guidance to Tempus’s real world data offering. 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.
Program Strategy Leader, MRD Portfolio Products
Company: Tempus
Location: Chicago, IL
Posted Aug 15, 2023
Tempus, a leading biotechnology company, is seeking a Scientific Strategy Leader to drive the development and commercialization of its MRD product portfolio. The role involves scientific program strategy, oversight of internal assays, evaluation of external partnerships, leading a cross-functional team, staying updated on advancements, collaborating with internal stakeholders, providing scientific support to the commercial team, analyzing market trends, ensuring regulatory compliance, driving scientific publications, and fostering a culture of innovation. The ideal candidate should have a PhD or MD in a relevant scientific field, proven experience in MRD measurement or molecular diagnostics, strong scientific leadership, excellent project management skills, business acumen, exceptional communication skills, ability to build relationships with key opinion leaders, and knowledge of regulatory requirements.
Medical Director, Informatics
Company: Tempus
Location: Chicago, IL
Posted Aug 22, 2023
The company is an equal opportunity employer and does not discriminate based on various characteristics.
Business Intelligence Engineer
Company: Tempus
Location: Chicago, IL
Posted Aug 21, 2023
The text discusses the use of AI in clinical care, specifically in precision medicine, to provide real-time, actionable insights to physicians. The company Tempus is mentioned as being on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. The text also mentions the need for advanced analytics dashboards and reporting, as well as the ability to solve new and interesting problems.
Senior Commercial Operations Analyst
Company: Tempus
Location: Chicago, IL
Posted Aug 21, 2023
The text discusses the role and responsibilities of a position within Tempus Compass, focusing on proposal development, contract negotiation, and change order management. The individual is expected to work collaboratively with various teams and stakeholders, demonstrate Tempus Compass values, and have a minimum of four years of experience in proposals, budget, contract, or change order development in a clinical research environment. The position requires excellent communication skills, independent judgment, and the ability to manage multiple tasks and priorities. The company is an equal opportunity employer.