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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Manager, Data Management Program Lead, Hematology - **Company:** BeiGene - **Location:** United States (Remote available) - **Experience:** Expert - **Salary:** $123,200.0 - $163,200.0 - **Contract:** Permanent contract - **Skills:** Microsoft Word, Microsoft Excel, Microsoft Outlook, Clinical Data Management, Databases, Data Validation, Data Visualization, Microsoft Software, Microsoft PowerPoint, SAS (Software), Data Processing, Data Management - **Published:** September 4, 2026 - **Apply:** https://beigene.wd5.myworkdayjobs.com/BeiGene/job/Remote-US/Manager--Data-Management-Program-Lead--Hematology_R36688 ## About the Role * 8+ years of experience in clinical data management in the pharmaceutical/biotechnology * Have excellent experience working in cross-functional team-oriented environments * Have strong oncology experience required * Have strong project management skills, 5+ years of experience as Lead Data Manager * Have experience developing Data Management standards * Good understanding of ICH and regulatory environment as it pertains to data management * During discussions with CST and other cross-functional teams, be capable of influencing others with decision making processes. * Working knowledge of one or more EDC systems, Medidata Rave preferred * Other duties as assigned Travel: Travel may be required as per business need, ability to travel domestically and internationally. Education Required: Bachelor's degree or equivalent in a health-related field preferred ## Description The Program Lead may be responsible for leading multiple clinical studies and/or multiple programs from the Data Management perspective. The role may also be responsible for process development and process improvement activities to ensure quality, compliance, consistency, as well as increase operational efficiency within Data Management., * When leading studies, be able to influence CST with expertise to mitigate the risks of the studies * Oversee the technical performance of the data managers to ensure timelines are met and data timepoints are finalized at the highest data quality. * Participate in Clinical Development taskforces and initiatives around standardization and technology, as needed * Collaborates effectively with other program leads in data management to ensure consistency in data handling and management of teams * Liaise with third-party vendors such as CROs and central laboratories in support of timelines and data-related deliverables * If assigned to a study, work with database builders to develop EDC databases, edit checks and reports * May regularly review and query clinical trial data as indicated in the Data Validation Specifications and Integrated Data Review Plan * Reviews and provides feedback on draft protocols, Statistical Analysis Plans, CSRs and other documents as required * May lead a product/program locally within Data Management as needed * Supports the Data Management standards and process improvement initiatives * Supports the development and maintenance of process documents (e.g., Standard Operating Procedures, Work Instructions) pertaining to Data Management activities * Develops and provides training to BeOne and FSP data management and cross functional team members on SOPs, process and standards as required. * May drive inspection readiness, quality compliance, and training initiatives pertaining to Data Management * May lead and/or oversee multiple clinical studies and programs * May function as the Data Management primary point of contact for all study team members and vendor partners * May oversee day to day activities of data managers working on clinical studies within a program * May serve as an active member of Clinical Study Teams * May work with other functions to manage timelines and ensure that data management deadlines are met * May create and maintain study specific data management documentation * May identify and troubleshoot operational problems, issues, obstacles, and barriers for studies, programs, and initiatives * Program Lead role, individual should ensure consistency within the DM practice, while working with other DMPLs * Other duties as assigned Computer Skills: Microsoft Applications (Outlook, Word, Excel, PowerPoint, Project) Working knowledge of more than three EDC systems, Medidata Rave required SAS Viewer and competencies in visualization tools. ## Related Videos - [Developing the Rich Text Editor for DeepL.com](https://www.wearedevelopers.com/videos/1172-developing-the-rich-text-editor-for-deepl-com) - [Times of (climate) crisis - How and why sustainable software is a must!](https://www.wearedevelopers.com/videos/988-times-of-climate-crisis-how-and-why-sustainable-software-is-a-must) - [Kubernetes and Microservices with Multi-Model Databases](https://www.wearedevelopers.com/videos/382-kubernetes-and-microservices-with-multi-model-databases) - [ZEISS & Microsoft - Building the Next Generation Medical Ecosystem in the Cloud](https://www.wearedevelopers.com/videos/424-zeiss-microsoft-building-the-next-generation-medical-ecosystem-in-the-cloud) - [Geometric deep learning for drug discovery](https://www.wearedevelopers.com/videos/264-geometric-deep-learning-for-drug-discovery) - [Kettle and Pot or Peas in a Pod? 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