Company

KatalystSee more

addressAddressFlorham Park, NJ
type Form of workFull-Time
CategoryInformation Technology

Job description

Responsibilities:
  • Creation of SAS programs to Develop or Validate SDTM/ADaM/TLFs.
  • Provide oversight for CRO SDTM/ADaM/TLFs deliverables for multiple studies and make sure efficiencies are gained at the project level.
  • Generate and/or review SDTM mapping specifications, annotated CRFs, ADaM specifications, Define.XML documents, and reviewer's guides per CDISC and FDA specifications and guidelines using standard tools and templates.
  • Demonstrate expertise in the SAS language, procedures, and options commonly used in clinical trial reporting - including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH.
  • Create all files, documents, and analyses necessary to support electronic submission(s) in an eCTD format, including ISS/Client.
  • Accountable for oversight of Statistical Programming deliverables on project level for inhouse and outsourced projects.
  • Manage all aspects of Statistical Programming deliverables for multiple studies/projects.
  • Support in the development and review of global standards, templates, processes, SOPs and Work Instructions.
  • Partner with cross-functional groups on timelines, vendor selection and CRO oversight.

Requirements:

  • BS or MS in Computer Science or Biostatistics.
  • Minimum of 5 years of industry experience in Statistical Programming to include oversight of CRO deliverables.
  • Expertise in the SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH.
  • Experience in the development and validation of CDISC SDTM and ADaM data models by transforming raw data into standard domains and development and validation of Tables/Listings/Figures.
  • Creation of all files, documents, and analyses necessary to support electronic submission(s) in an eCTD format, including ISS/Client.
  • Hybrid work arrangements will allow work from home combined with your presence on-site at our US HQ in Florham Park, NJ.
  • Good knowledge of 21CFR11 and GCP.
  • Good knowledge of Drug development process and Biostatistics
  • Current knowledge in technologies and tools related to Statistical programming or Biostatistics.
Refer code: 8438701. Katalyst - The previous day - 2024-03-03 10:02

Katalyst

Florham Park, NJ
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