Senior Data Management Lead (UK, Ireland, Spain, Romania, Poland)

The Senior Data Management Lead provides leadership and expertise in all aspects of Data Management. Develop and manage timelines for study data deliveries, including Go-Live, Interim Deliveries and Final DB Lock. Collaboration with the relevant functions (Clinical, Biostatistics, Database Programming, Medical, Medical Writing etc.) across all geographies. Data Management single point of contact to ensure that the contracted Data Management deliverables are being met – specifically in terms of timeliness, financial management and quality.

The Senior Data Management Lead can competently and independently lead large, complex projects and/or programs with little to no guidance from their Line Manager and/or Subject Matter Experts. Senior DMLs may act as a mentor for ADMLs, DMLs and other Senior DML peers.

May act as Project Leader for projects, involving only Global Data Operations service.QualificationsRole requirements:

Leadership skills that include:Building and leading global (virtual) teams.Ability to work effectively with and motivate virtual teams.Ability to negotiate and influence in order to achieve mutually beneficial results.Proven problem solving skills.Strong ability to manage multiple and varied tasks with enthusiasm, prioritize workload with attention to detail.Excellent interpersonal, oral and written communication skills.Excellent presentation skills.Ability to travel as required.Business / Operational skills that include:Strong customer focus, ability to interact professionally within a client organization.Understanding of Parexel project financial tools, reports and processes for management of project financials with regards to forecasting, revenue recognition, scope of work and department budget for assigned projects.Understanding of Global Data Operations tasks, specifically within Data Management and Database Programming and relevant data standards.Sound awareness of relevant regulations, including ICH-GCP, 21CRF11.Excellent technical skills including but not limited to the knowledge of Clinical Trial/Data Management Systems, PMED, IVRS.Basic knowledge of SAS.Knowledge and Experience:Substantial experience in clinical research.Proven record of leading project and program teams in a technical/programming or data processing environment.Strong understanding of cross functional activities.Strong customer service focus.Robust knowledge of ICH-GCP Guidelines and local regulatory requirements.Education:Bachelor’s degree and / or other qualifications in a science or industry related discipline.Competent in written and oral English.