Clinical Statistical Programmer

Our requirements

• 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

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

This is how we organize our work

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

• 1.
  Screening Interview
• 2.
  Technical Assessment
• 3.
  Technical Interview
• 4.
  Offer

NoyMed Corp