Statistical Programmer III
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Statistical Programmer III
Ref No.: 17-00764
Location: East Hanover, New Jersey
Start Date: 03/08/2017
Title: Statistical Programmer III
Job#: 4516490
Location: East Hanover, NJ
Duration: 6+ months

This role is 100% on-site in East Hanover, no work from home arrangements will be made.
Responsibilities
  • Candidate should be able to perform development of analysis dataset, generation of tables, listings and graphs from both internal and external data sources.
  • Review/Develop programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician
  • Review and provide feedback on statistical analysis plan, output shells, CRF, edit checks and other relevant trial documents
  • Program according to specifications, analysis datasets, pooled datasets, listings, and figures for clinical trials and submission activities
  • Support quality control and quality audit of deliverables
  • Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities
  • Track clinical trial milestones for statistical reporting deliverables.
  • Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation
Skills
  • Minimum of 5+ years previous SAS programming and development. Previous pharmaceutical SAS experience is mandatory.
  • Must be able to demonstrate experience in generation preparation of analysis dataset, generation of both safety and efficacy tables, listings and graphs and strong validation skills. Good programming experience in pooled analysis is a plus.
  • Expert knowledge/experience in SAS software.
  • Good knowledge of drug development process, SDMT, ADaM IG, CDISC standards.
  • Ideal candidates should be able to demonstrate clinical trial data flow, especially in Oncology.
  • Excellent verbal and written communication skills.
  • Good organizational interpersonal and diplomacy skills.
  • Continuous improvement mentality and attention to detail.
  • Consultant will be working with existing code and modifying or adding to it. Will be working in a team environment with multiple programmers. S/he develops and complies with project/study standards and specification following internal and regulatory guidelines. S/he maintains records for all assigned projects and archives trial/project analysis and associated documentation.
  • Clinical pharmacological trial experience is preferred but not required.
  • Intermediate knowledge of office tools
  • Fluent English (oral and written)
  • Excellent in people interaction and be a collaborative team player.
Education
Minimum of BA/BS or equivalent experience in mathematics, statistics, computer science or life science or related field(s).