Responsibilities: Lead the management of CDM deliverables in coordination with internal and external cross-functional teams. Lead by providing CDM expertise for data coordination, collection, and cleaning to efficiently ensure high quality data. Perform the execution of end-to-end Data Management activities (e.g., eCRF development, Data Review, study lock) for multiple studies across therapeutic areas and/or indications. Develop and manage data management timelines to ensure study goals and activities are met. Oversee External Data Management activities by providing project level support of External Data Management tasks (development of Data Transfer Plans, coordination of file transfers to meet study deliverables etc.). Anticipate obstacles and difficulties of stakeholders and staff and acts upon them or escalates accordingly in order to meet team goals. Manage the development and finalization of CDM documents to be filed in the eTMF. Review and manage the eTMF for completeness and accuracy, ensuring inspection readiness. Serve as a primary point of contact for internal and external study team members in relation to all Data Management activities. Ensure completeness, accuracy, and consistency of clinical data and data structure across all projects on an ongoing basis. Responsible for data review, query management, and metric report delivery to study teams. Coordinate study timelines and database snapshots for analysis and safety review meetings. Participate in and/or represent CDM during internal audits as well as Health Authority audits and inspections. Participate in the development, review, and implementation of processes, policies, SOPs, and associated documents affecting CDM. Participate in CDM and cross-functional initiatives. Proactively provides input to continuous improvement activities within Clinical Data Management and provides the relevant support for implementation. Flexible to changing priorities, detail-oriented, works well under pressure, and able to take on unfamiliar tasks. Demonstrates an ability to prioritize and delegate effectively. Demonstrates ability to assume expanded scope of responsibility with respect to volume and complexity of clinical project work. Works collaboratively with Clinical and Statistical Programming, Clinical Operations, Biostatistics, and others study team members to meet project deliverables and timelines. Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other clinical data management systems). Experienced with industry wide thesauri/dictionaries such as MedDRA and WHODD. Demonstrates excellent verbal and written communication skills, including the ability to clearly describe critical technical CDM aspects to non-CDM staff. Training and mentoring of junior CDM staff. Communication and escalation of project level issues including processes, timelines, resourcing, performance, etc. Requirements: Master's and 4+ years of Data Management experience Bachelor's and 6+ years of Data Management experience. High School Diploma/GED and 10+ years of Data Management experience. Experience as independent lead in managing clinical data management deliverables for regulatory filings. 6 years of relevant industry experience with clinical trials and a successful track record of leading through influence, working across complex, global organizational matrices. Experience in Industry Standards Guidelines (e.g., CDISC) in either the collection (CDASH), tabulation (SDTM), or analysis (ADaM) models. Strong knowledge of industry-leading EDC tools (e.g., Medidata Rave, Veeva EDC, Medrio EDC, Oracle, TrialGrid, etc.) and well versed in industry trends and emerging technologies supporting data collection.