SAS Programmer

в NoyMed CRO (посмотреть профиль)
Город Armenia
Опубликовано 26.08.2021
Категория Биоинформатика

Обязанности

NoyMed is looking for experienced Snr. SAS Programmers to join our expanding team by working remotely. 

 

  • Develop specifications for analysis datasets in consultation with Biostatistician
  • Follow the Study Data Tabulation Model (SDTM) Implementation Guide, write specifications for SDTM datasets
  • Follow statistical analysis plans and the Analysis Data Model (ADaM) Implementation Guide, write specifications for analysis datasets
  • Follow specifications, develop algorithms and write programs to create datasets
  • Implement entire programming process
  • Develop the programs using SAS to produce Tables, Listings, and Graphs asper the specifications indicated in Statistical Analysis Plan
  • Implement installation of VCS client applications and/or plug-ins
  • Implement checkout, check-in, update, merge of the working copies
  • Independently check data listings, summary tables and graphs
  • Import and export SAS data
  • Perform programming validation to assure accuracy, reliability and consistency
  • Assist data management group in performing data edit checks
  • Understand and conduct work consistent with GCP, ICH, 21 CFR part 11, internal SOPs and training, and international regulatory requirements

Требования

  • At least a Bachelor degree in Computer Science or a related field
  • 3+ years relevant work experience
  • Excellent English knowledge
  • 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
  • Experience in reports and query development, especially for data validation and data quality assessment; experience with electronic data capture (EDC) and database management systems (e.g., REDCap, Medidata, TrialMaster, Inform, etc.)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 the 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

Зарплата

не указано

Условия

To apply for this position please send your CV to career@noymed.com. 

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