IQVIA
IQVIA
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Senior Statistical Programmer - FSP

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SeniorFull-time
#445498·Dodano 7 dni temu·1
Źródło: IQVIA
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Tech Stack / Keywords

SASSAS MacrosR ProgrammingCDISCCDASHSDTMADaM

Firma i stanowisko

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Wymagania

  • BSc in Computer Science, Mathematics, Statistics or related field with relevant experience.
  • At least 5+ years of experience in clinical or statistical programming within CRO/pharmaceutical environments.
  • In-depth understanding of clinical/statistical programming processes and standards.
  • Extensive experience with SAS, including development and use of Macros.
  • Hands-on experience in R Programming is mandatory.
  • Advanced knowledge of CDISC standards (CDASH, SDTM, ADaM).
  • Proven experience leading programming for pooled and exploratory analyses across multiple clinical studies.
  • Ability to work independently and in team settings, managing own timelines.
  • Experience working in cross-functional, multicultural, international clinical trial teams.

Obowiązki

  • Collaborate with study teams to design data structures and specifications for ADaM datasets, tables, figures, listings, and analysis submission content.
  • Ensure quality and accuracy of clinical data for regulatory submission (SDTM, ADaM, define.xml).
  • Lead efforts for pooled and exploratory analyses with statisticians and clinical programming teams.
  • Oversee specification and delivery of ISS and ISE datasets and associated outputs when not provided by CRO.
  • Design and implement complex SAS programs for analyzing clinical trial data in CDISC ADaM format.
  • Develop global tools to increase Statistical Programming group efficiency and capacity.
  • Plan and execute project activities to meet timelines with high-quality deliverables.

Additional tasks:

  • Collaborate with CR&D staff on data analysis requests.
  • Perform statistical analyses supporting regulatory responses, integrated summaries, publications, presentations, and clinical trial planning via exploratory analyses.

Inne informacje

IQVIA maintains a zero-tolerance policy for candidate fraud. False statements, misrepresentations, or material omissions during recruitment result in disqualification or employment termination per applicable law.

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