We are seeking an experienced Senior Manager, Technical Clinical Data Management to take full accountability for end-to-end data management lifecycle activities across assigned clinical trials. In this dual-function role, the individual will serve as the primary Data Management Study Lead, managing timelines, cross-functional communication, risks, and deliverables while also applying hands-on technical expertise.  Candidate will combine strong clinical data management leadership with the technical ability to design efficient, scalable solutions that improve data quality, accelerate issue resolution, and support timely study delivery.Key Responsibilities:
Clinical Data Management Leadership & Technical Operations Leadership & Study OversightRepresent Data Management on the Clinical Study Team, lead study communications, and manage expectations with the Data Management CROOversee all activities defined in the Data Management Plan (DMP) and ensure study deliverables meet quality and timeline expectationsTechnical OperationsAdvance vendor oversight by applying data intelligence to identify trends, strengthen performance monitoring, and improve operational efficiencyPartner with IT to streamline external data transfers and integrate data across systems for cross-functional useVendor & Stakeholder Management Oversee outsourced CDM vendors and ensure performance aligns with Deciphera standardsReview vendor invoices as applicableCollaborate with cross functional team on data deliverablesLeadership, Process & Continuous Improvement Enhance CDM processes and strengthen cross functional collaborationSupport department initiatives as neededInspection Readiness, Quality & Metrics Lead CDM inspection activities and manage findings to resolutionEnsure CDM documentation is complete and filed in the TMFOther duties and responsibilities as assigned
