IQVIA

Senior Statistical Programmer - FSP

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SeniorOn-site·WarszawaFull-time

#445498·Dodano 29 dni temu·2

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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