Associate Director, Clinical Data Management

Exciting time to be joining Deciphera as we continue to build an amazing Clinical Data Management Team. Come join our dedicated and forward-thinking DM group as we embrace innovative technologies and processes in this evolving industry. We are seeking an Associate Director of CDM to lead clinical data management activities across one or more clinical programs or therapeutic areas within the portfolio. This position will report to the Director or Sr. Director Head, of Clinical Data Management.What You'll Do:Ensure the data quality and data integrity for highly complex or pivotal clinical studiesMay manage escalations and ensure that optimal relationships are developed with the outsourced CDM vendorMay help select and manage CDM vendors and ensure their performance is consistent with Deciphera standardsMay review and approve invoicesForecast timelines and resources required to complete study-specific tasks on time and with high qualityWork collaboratively with stakeholders in Medical Affairs, Regulatory, PV to determine dates of program data deliverablesProvide expert CDM guidance to study teams, vendors and managementResolve complex technical or procedural issues and manage the escalation of issuesCommunicate issues and ongoing study and program updates to managementMay oversee and develop team of CDM staffMay identify and evaluate modern technology and propose to managementMay contribute to projects involving standard ways of collecting and harmonizing clinical trial data, such as standard eCRFs, standard validation checks and conventionsEnsure CDM activities are executed in accordance with all relevant SOPs and study plansEnsure CDM documentation is filed according to SOPs and the study plansSupport inspection activities and manage any findings to resolutionParticipate in the development and revision of Standard Operating Procedures (SOPs)Define metrics to measure clinical trial database quality, site and vendor performance and implement those metrics in the clinical trialsMay propose and define Key Risk Indicators (KRIs) and Quality Threshold Limits (QTLs) related to clinical trial data and sites.Analyze metrics across projects and programs; escalate or inform management and cross functional colleagues to trendsFacilitate resolution of operational problems, issues, obstacles and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholdersAssist with development of therapeutic area standards for Case Report Forms and Edit ChecksFunction as the CDM subject matter expert for process related questions from other Clinical Data Managers, cross functional colleagues and business improvement teams