8 Apr 2026

Senior Statistical Programmer (FSP - Permanent Homebased)

IQVIA

Amsterdam

8 Apr 2026

Apply

Senior Statistical Programmer role dedicated to a major client through IQVIA's FSP partnership, focusing on clinical data analysis using SAS and CDISC standards. Requires at least 5+ years of experience in clinical/statistical programming within the CRO/pharmaceutical environment. Responsibilities include designing and implementing SAS programs, ensuring submission readiness, and collaborating with study teams.

RemoteFull-timeSeniorSASSAS Macros

Senior Statistical Programmer (FSP - Permanent Homebased)

Apply

RemoteFull-timeSeniorSAS

Salary

Not specified

Work Location

Amsterdam, North Holland, Netherlands, NL

Work Model

Remote

Experience Required

5 years

Employment Type

Full-time

Experience Level

Senior

Core Qualifications

Technical (Must-have)

SASSAS MacrosCDISCCDASHSDTMADaMGCPICH

Soft Skills

problem-solvingteamworkcommunicationleadershiptime management

Tools (Must-have)

SAS Software

Key Responsibilities

•Collaborates with study teams to design data structure and specifications for ad hoc and study deliverables including ADaM datasets, Tables, Figures, Listings and Analysis Submission content.
•Collaborates with study teams to ensure the quality and accuracy – thus submission readiness – of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml).
•Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead and/or study statisticians as well as with clinical programming team and their collection of legacy data.
•Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO.
•Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.
•Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group.
•Works closely with clinical study teams to plans and executes activities to ensure project timelines are met with high quality deliverables.
•Collaborates with CR&D staff regarding data analysis requests.
•Performs additional statistical analyses including support responses to regulatory agencies, generate integrated summary of safety and efficacy, support publications and presentations, support planning and reporting of clinical trials via exploratory analyses of available data.

Senior Statistical ProgrammerClinical ProgrammingStatistical ProgrammingSASCDISCHealthcareCROPharmaceuticalRemoteFull-time

Key Responsibilities

•Collaborates with study teams to design data structure and specifications for ad hoc and study deliverables including ADaM datasets, Tables, Figures, Listings and Analysis Submission content.

•Collaborates with study teams to ensure the quality and accuracy – thus submission readiness – of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml).

•Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead and/or study statisticians as well as with clinical programming team and their collection of legacy data.

•Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO.

•Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.

•Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group.

•Works closely with clinical study teams to plans and executes activities to ensure project timelines are met with high quality deliverables.

•Collaborates with CR&D staff regarding data analysis requests.

•Performs additional statistical analyses including support responses to regulatory agencies, generate integrated summary of safety and efficacy, support publications and presentations, support planning and reporting of clinical trials via exploratory analyses of available data.