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Senior statistical programmer (m/w/d)

Bristol (City of Bristol)
IQVIA
Statistical programmer
Posted: 21h ago
Offer description

Overview

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based). Responsibilities

Import data from various sources Program quality control checks for source data and reporting data issues Interpret project level requirements and develop programming specifications Write programming code following established Good Programming Practices Program SDTM and ADaM datasets Program to create statistical analysis tables, listing and figures Validate datasets and all statistical outputs per prescribed gate checks Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines Use and promote the use of established standards, SOPs, and standard methodologies Export data and clinical study report materials Provide training and mentoring to team members and department staff We offer exposure to cutting-edge in-house technology and opportunities to work on global projects across therapeutic areas, with development opportunities and mentoring to progress your long-term career in the direction you choose. Qualifications

Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science 5+ years of experience in a Statistical Programmer role from CRO/Pharma with ADaM/SDTM/TLFs Excellent accuracy, attention to detail, problem solving, organizational as well as interpersonal communication Experience in SAS programming within the CRO/Pharma/Biotech/Healthcare industries Knowledge of statistics and routine to complex analytical skills Focus on quality, accuracy, and completeness of work activities Excellent communication skills Good understanding of Good Clinical Practice and ICH guidelines Ability to independently lead (or have lead potential) and estimate programming scope of work, manage resources, communicate status, and meet project timelines Take initiative and reliability to complete tasks with integrity Self-awareness to recognize when negotiation or assistance is needed Ability to establish and maintain effective working relationships with coworkers, managers, and clients This role is not eligible for UK visa sponsorship

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