Manager, Biostatistics

Manager, Biostatistics - Permanent - w / m / d Global BiostatisticsHome-Based/Hybrid: GermanyJoin us on our exciting journeyThe Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.Due to continued growth, we are seeking new brave minds to join our award winning and innovative department. You will have the opportunity to work globally and across a variety of therapeutic areas. IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.Job Overview:As a Manager for the Biostatistics department, you will provide direction and guidance in carrying out project assignments, interfacing with clients and other internal departments, and applying statistical methods to project work.With site/staff level of visibility, you will manage a team of Biostatistics staff and provide training, guidance, and mentorship to staff members.Along, with communicating on project progress, staffing concerns, including resource allocation with the Director, BiostatisticsYou will perform expert reviews and participate as senior statistician on major projects, including developing/reviewing protocols, preparing analysis plans, overseeing the conduct of analyses, and preparing integrated clinical and statistical reports.Requirements:BSc or MSc degree in Biostatistics or related field and between 5-7 years’ relevant experience within the life-science industry, along with at least 1-year experience in supervising/managing staffFamiliarity with most complex statistical methods that apply to Phase I-IV clinical trialsIn-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesFamiliarity with moderately complex statistical methods that apply to applicable clinical trialsStrong working knowledge of SASFrom camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues. What is in it for you?Global exposureVariety of therapeutic areasCollaborative and supportive team environmentAccess to cutting-edge in-house technologyExcellent career development and progression opportunitiesWork-Life BalanceJOIN USEmbrace your curiosity and grow your career in an exciting environment where development is a priority.Think boldly and disrupt conventional thinking.Enjoy what you do.Whatever your career goals, we are here to ensure you get thereIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at