Statistical Programmer II

Veeda Lifesciences is seeking a Statistical Programmer II based in Europe for its growing international hematology/oncology Clinical Trials program. This is a full-time job. Job overview:The Statistical Programmer II is responsible for providing clinical programming expertise and support to clinical studies across multiple therapeutic areas, as part of the Company’s global Phase I-III program. The role will contribute to the development, validation, and delivery of high-quality clinical trial programming outputs in accordance with CDISC standards, applicable regulations, and Company procedures. Main responsibilities:Write, maintain, and validate SAS programs to create templates and macros for data cleaning and reportingDevelop SAS programs to create and validate SDTM datasets and perform SDTM quality control under supervisionWrite SAS programs, under senior supervision, to develop ADaM datasets and ADaM TFLs in accordance with CDISC standards and implementation guidelinesProgram edit checks in accordance with approved specificationsPerform data transfers to external recipients and ensure the accuracy and integrity of transferred dataCollaborate closely with Data Management, Statistics, and other stakeholders to ensure accurate, timely, and high-quality deliverablesContribute to the delivery of clinical programming activities across studies and therapeutic areasComply with the Company’s Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protectionWork according to established SOPs, guidelines, regulations, and ethical principles in daily practice Job Requirements:BSc in Statistics, Mathematics, Biostatistics, Data Analysis, Data Science, or a related fieldMSc in Statistics, Mathematics, Biostatistics, Data Analysis, Data Science, or a related field is desirableAt least 5 years of SAS programming experience supporting CDISC-compliant clinical studies within a CRO, pharmaceutical company, or equivalent institutionExcellent command of English, both oral and writtenStrong knowledge of Base SAS, SAS/STAT, SAS Graph, and SAS Macro LanguageGood knowledge and understanding of CDISC requirements and standardsExcellent statistical programming skillsExpertise in manipulating and analyzing SAS datasetsHands-on experience developing and validating clinical trial datasets and programming outputsExperience with SDTM development and quality controlExperience developing ADaM datasets and ADaM TFLs in accordance with CDISC standardsExcellent analytical and computer skillsStrong communication and interpersonal skillsAbility to work effectively in a collaborative and multidisciplinary environmentGenuine interest in clinical development and clinical researchStrong organizational, problem-solving, and decision-making abilitiesAbility to work according to established SOPs, guidelines, regulations, and ethical principles in daily practiceSAS Certified Programmer qualification is desirable Join us to be part of a multidisciplinary team of highly skilled scientists and healthcare professionals in the forefront of Clinical Research within a friendly work environment.