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Position: Senior Biostatistician
Institution: IQVIA
Location: Antwerpen, Frankfurt, Berlin, Irene, London, Belville, Reading, Brussels, Bloemfontein, Belgium, Germany, Netherlands, United Kingdom, South Africa
Duties: Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. Interpret analyses and write statistical sections of study reports.Provide training, guidance and mentorship to lower level and new staff
Requirements: PhD in Biostatistics or related field and 3yearrelevant experience/Master's degree in Biostatistics or related field and 6 years relevant experience/Bachelor's degree in Biostatistics or related field and 8 years relevant experience; or equivalent combination of education, training and experience; In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Familiarity with moderately complex statistical methods that apply to applicable clinical trials; Strong individual initiative; Strong organizing skills; Strong working knowledge of SAS computing package
   
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Start right here at IQVIA. Enter Keyword Enter Location Search Jobs Senior Biostatistician - UK / Europe / South Africa Apply now Reading, England Full time R1137123 Date Posted: 07/17/2020 Job description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.PURPOSEDevelop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. Interpret analyses and write statistical sections of study reports.Provide training, guidance and mentorship to lower level and new staff.RESPONSIBILITIESCoordinate the development of analysis plans, table shells, programming and table specifications, the production of tables, listings and figures, data review and statistical analysis.Perform protocol development, sample size calculation, protocol and CRF review.Advise data management staff on database design, and critical data. May advise on validation checks.Write statistical sections of integrated reports.Provide expert statistical input into and review of statistical deliverables (i.e. analysis plans, table shells, programming and table specifications, data review, tables, listings, figures and statistical sections for integrated reports) and data management deliverables (i.e. database design, validation checks and critical data).Act as statistical team lead for single complex studies or groups of studies.Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage scope, and provide revenue and resource forecasts for single studies. May manage project budget and resource requirements.Perform the review of RFPs and QIPs, prepare proposal text and attend bid defense meetings.Manage customer relationships.Provide training and guidance to lower level and new staff.REQUIRED SKILLS AND ABILITIESExcellent written and oral communication skills including grammatical/technical writing skillsExcellent attention and accuracy with detailsIn-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Familiarity with moderately complex statistical methods that apply to applicable clinical trialsStrong individual initiativeStrong organizing skillsStrong working knowledge of SAS computing packageFamiliarity with other relevant statistical computing packages such as nQueryStrong commitment to qualityAbility to effectively manage multiple tasks and projectsAbility to provide and accept direction of lead team membersAbility to solve moderately complex problemsAbility to establish and maintain effective working relationships with coworkers, managers and clientsWorking knowledge of relevant Data Standards (such as CDISC/ADaM)MINIMUM REQUIRED EDUCATION AND EXPERIENCEPhD in Biostatistics or related field and 3yearrelevant experience / Master's degree in Biostatistics or related field and 6 years relevant experience / Bachelor's degree in Biostatistics or related field and 8 years relevant experience; or equivalent combination of education, training and experienceRequires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.Join UsMaking a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.Forge a career with greater purpose, make an impact, and never stop learning. Apply now Save job Remove saved job Recently Viewed Jobs No Recently viewed jobs. View all opportunities. Explore location Share this job Twitter LinkedIn Facebook Learn more about IQVIA Our Company At IQVIA, we want to help customers take healthcare further than ever before. Life at IQVIA Our work is important. It's challenging. And we're committed to working together to make a difference. Join IQVIA’s Talent Network Register today and we'll let you know when positions that match your career interests become available. 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