Lead Data Manager

<p style="text-align:left"><span><b><span>Passionate about precision medicine and advancing the healthcare industry?</span></b></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span>Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus&#39; 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.</span></span></p><p style="text-align:inherit"></p><p>Tempus&#39; 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.</p><p></p><p>We&#39;re looking for an experienced Senior Clinical Data Manager to help us design and execute on clinical evidence studies with the mission of delivering personalized care to cancer patients.</p><p></p><p><u>What You’ll Do</u></p><ul><li>Responsible for all data management activities in support of clinical studies, including:<ul><li>eCRF development</li><li>Database build activities, including database development, edit check specifications and performance of user acceptance testing</li><li>Data collection, data cleaning and reporting</li></ul></li><li>Document project-specific data management, data validation, data transfer and data entry guidelines to ensure appropriate, consistent, and efficient processing of data in collaboration with key stakeholders</li><li>Develop and execute data validation programs and generate queries on potentially discrepant data</li><li>Design, develop and execute programs to support data reporting, central monitoring, identification of patients and data transformations.</li><li>Responsible for the coordination and execution of the review and verification of all data collected for a project, including reconciliation of external data (e.g., central laboratories, local laboratories) to ensure all data is correct, complete, and logical</li><li>Interface with internal functional teams responsible for data quality and delivery to ensure a robust, quality regulatory-grade data pipeline</li><li>Responsible for documentation activities, including development and maintenance of the data management project file and close out activities, including locking and archival of the final project database</li><li>Contribute to department process improvement efforts and authorship and/or review of department SOPs</li></ul><p><u>Required Knowledge And Skills</u></p><ul><li>Bachelor&#39;s degree in an analytical or healthcare related field</li><li>7&#43; years of relevant industry experience in clinical data management and analytics</li><li>3&#43; years of using programming techniques or software to aggregate, extract, and analyze data across multi-table relational database schemas</li><li>Expert knowledge of Data Management processes, efficient design/build of an EDC data management system and other Clinical Trial/Data Management System</li><li>Knowledge and understanding of regulations and industry-adopted data standards, such as CDISC SDTM and CDASH</li><li>Understanding of ICH GCP as well as general knowledge of industry practices and standards</li><li>Knowledge and understanding of regulatory requirements and expectations for clinical data systems including 21 CFR Part 11</li><li>Advanced knowledge of MS Suite and Google document applications</li><li>In-depth understanding of clinical data management systems (e.g. Medrio, Medidata Rave)</li><li>Ability to compile, organize and analyze various types of data</li><li>Developing and adhering to SOPs that follow industry guidelines for effective and compliant data handling, archiving and modifying data management infrastructures</li><li>Excellent analytical and problem solving skills</li><li>Highly organized and systematic, superb attention to detail and ability to complete tasks with a high degree of accuracy</li><li>Ability to effectively prioritize in a challenging, rapidly changing, and time sensitive environment with minimal guidance</li><li>Proven ability to learn new things continuously and quickly and navigating ambiguity</li><li>Ability to lead others work product either in line management or matrix reporting</li><li>Ability to work independently and as part of a multi-disciplinary team</li></ul><p></p><p><u>Nice To Haves</u></p><ul><li>Bachelor’s degree in pharma science, research methodology, computer science, computer engineering, or data science</li><li>Experience working with EMRs such as EPIC</li><li>Experience working with Google Looker and dbt</li><li>Oncology experience (Breast Cancer, Lung cancer, Hematologic Cancers etc.)</li></ul><p></p><p>#LI-NK1</p><p style="text-align:inherit"></p><p style="text-align:left">We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. </p>