Clinical Data Manager

We are seeking an experienced Clinical Data Manager to join our team at Tempus. In this role, you will be responsible for managing all data activities related to clinical studies, including eCRF development, database build activities, data collection, cleaning, and reporting. You will also be involved in developing and executing data validation programs, as well as designing and executing programs for data reporting and transformations. Additionally, you will ensure the accuracy and completeness of all collected data and collaborate with internal teams to maintain a high-quality data pipeline.

• Responsible for all data management activities in support of clinical studies, including eCRF development, database build activities, data collection, data cleaning, and reporting
• Document project-specific data management, data validation, data transfer, and data entry guidelines
• Develop and execute data validation programs and generate queries on potentially discrepant data
• Design, develop, and execute programs to support data reporting, central monitoring, identification of patients, and data transformations
• Coordinate and execute the review and verification of all data collected for a project, including reconciliation of external data
• Interface with internal functional teams responsible for data quality and delivery
• Responsible for documentation activities, including development and maintenance of the data management project file and close out activities
• Contribute to department process improvement efforts and authorship and/or review of department SOPs

• Bachelor's degree in an analytical or healthcare related field
• 5+ years of relevant industry experience in clinical data management and analytics
• 3+ years of using programming techniques to aggregate, extract, and analyze data across multi-table relational database schemas
• Expert knowledge of Data Management processes, efficient design/build of an EDC data management system and other Clinical Trial/Data Management System
• Knowledge and understanding of regulations and industry-adopted data standards, such as CDISC SDTM and CDASH
• Understanding of ICH GCP as well as general knowledge of industry practices and standards
• Knowledge and understanding of regulatory

• Competitive salary and compensation package
• Opportunity to work in the field of precision medicine and advance the healthcare industry
• Access to Tempus' proprietary platform for real-time, actionable insights in healthcare
• Chance to contribute to clinical evidence studies and deliver personalized care to cancer patients
• Responsibility for all data management activities in support of clinical studies
• Development and execution of data validation programs
• Design and execution of programs for data reporting, central monitoring, and data transformations
• Coordination and verification of all data collected for a project
• Interface with internal functional teams for data quality and delivery
• Documentation activities and maintenance of data management project files
• Contribution to department process improvement efforts and authorship/review of department SOPs
• Opportunity to work with industry-adopted data standards and regulations
• Advanced knowledge of MS Suite and Google document applications
• In-depth understanding of clinical data management systems
• Ability to compile, organize, and analyze various types of data
• Excellent analytical and problem-solving skills
• Highly organized and systematic with superb attention to detail
• Ability to work independently and as part of a multi-disciplinary team
• Opportunity for continuous learning and growth
• Equal opportunity employer with a commitment to diversity and inclusion.