Clinical Statistical Programmer

Expected, SAS Optional, SQL Operating system, Windows, Linux Your responsibilities, Understand and conduct work consistent with GCP, ICH, 21 CFR part 11, internal SOPs and trainings, and international regulatory requirements, Lead, or perform leading role on statistical programming activities in order to maintain project plan, track daily status updates and timelines within the team, as well as efficient communication methodology with clients, Responsible for accuracy, traceability and reproducibility of data, quality and reliability of deliverables of the project., Develop and validate specifications for SDTM datasets and analysis datasets follow, SDTM and ADaM Implementation Guides, statistical analysis plans, Develop and validate algorithms and programs to create datasets, Develop complex SAS macros in order to automate and standardize routine processes, Develop, upgrade and validate the programs to produce Tables, Listings, and Graphs At least Bachelor's or Master degree in Computer Science or a related field 3-5 or 5+ years’ relevant work experience, Excellent English skills, Strong sense of discipline and responsibility, In-depth understanding of data collection, data flow management, data quality, data extraction and data standards (knowledge of CDISC standards for CDASH, SDTM and ADaM a plus), Experience with multiple programming languages (SAS programming language, R, SQL or other languages/tools as required, SAS Certification desired), including the creation of data entry and query screens/processes and data quality checks, In-depth knowledge of research processes, clinical operations, and data quality management, Strong attention to detail and demonstrated proficiency in quantitative and qualitative analyses, Ability to manage multiple projects, tasks, and priorities; work independently with minimal supervision and execute tasks to completion without a great deal of direction, Experience in training users in operation of clinical trials software and tools, Ability to exercise judgment, initiative, and resourcefulness in making decisions in consultation with clinical research personnel, and independently if necessary, Demonstrated strong teamwork and organizational skills; outstanding interpersonal and communication skills Team size, 50-100 This is how we work, in house, at the client's site, you focus on a single project at a time What we offer, Employees on fixed-term contracts are entitled to unlimited Paid Time Off (PTO), Company provided laptop with keyboard and mouse Benefits, remote work opportunities, flexible working time, employee referral program Recruitment stages, Screening Interview, Technical Assessment, Technical Interview, Offer NoyMed Corp, NoyMed, founded in 2017, is an expert niche Biometrics CRO with full ClinOps capabilities supporting studies from Phase I-IV working with Pharmaceutical, Biotechnology, Medical Device companies and Research Institutes globally.