Associate Director, Data Management

Department: 106300 Biometrics Location: San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients.Our work is rewarding - both professionally and personally - because we are making a difference. We are passionate about what we do. We are seeking talented individuals who will thrive in our collaborative, diverse, fast-paced environment and share in our mission - to identify, develop and deliver life-changing therapies to people living with rare disease. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community. At Travere Therapeutics, we are in rare for life. We continue to courageously forge new paths as we move toward a common goal of elevating science and service for rare patients*.* Job Summary The Associate Director, Data Management will be responsible for overseeing the start-up and execution of several trials with a CRO or in-house to ensure data quality and integrity. The individual will provide data management clinical development program leadership and will perform a variety of complex tasks to ensure complete, accurate, high quality, and regulatory compliant data in support of publications and regulatory submissions. Responsibilities: Leadership and accountability for data management deliverables within a given development program. Develop, maintain and execute data management timelines for a given development program. Data Management Leadership in program related audits and regulatory inspections. Lead and participate as data management subject matter expert at Study Management Team meetings. Identify gaps in existing data management processes within a program and champion process change efficiencies. Serve as Lead CDM to manage and provide daily oversight of CROs and third-party vendors in relation to DM to ensure successful clinical trial implementation and execution to completion. Perform ongoing data review of clinical data to identify data discrepancies, general data trends, and corresponding resolutions as part of oversight over the CROs. Review data for protocol deviation identification, as well as coding, and user acceptance testing of database. Review documents produced by vendors and other departments. Work cross-functionally with other departments within the company assessing and understanding their needs and attend clinical trial project team meetings as Lead CDM. Strategize and plan for database locks and multiple deliverables across numerous programs. Provide input on the development of standard operating procedures (SOPs) and study protocols from a data management perspective. Provide guidance to clinical data management personnel on assigned projects. Set-up, maintain and archive data management related project documentation (i.e., Data Management Plan, CRF Completion Guidelines, etc.). Independently monitor own activities and project status for successful project deliverables according to timelines. Adhere to budgets and timelines. Ensure project is in reasonable state of inspection readiness and compliance. Work with minimal supervision. Experienced in designing clinical trials utilizing CDASH and SDTM standard terminology. Strong technical skills and experience with managing system integrations across data platforms. Additional duties assigne