Senior Statistical Programmer – FSP

Parexel

Senior Statistical Programmer providing technical expertise for the conduct of clinical trials. Working independently on programming activities related to analysis and reporting.

Posted 5/23/2026full-timeWarsaw • 🇵🇱 PolandSenior💰 PLN 200,000 - PLN 278,000 per yearWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

SASprogramming validationanalytical programmingclinical data structureCDISC standardsrelational databasesADaMData Definition Tablee-submissionupstream data processing

Soft Skills

leadershipteam collaborationcommunicationproblem-solvingattention to detailefficiency improvementindependencestrategic thinkingproject managementvendor interaction

Tools & Technologies

MS OfficeXMLPinnacle 21eDCworkflow management

Industry Keywords

clinical programmingpharmaceutical clinical developmentregulatory compliancestatistical terminologyclinical testsmedical terminologyprotocol designs

About the role

Key responsibilities & impact

Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures
Perform programming validation to ensure quality of analysis datasets and programming outputs
Provide programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis
Support the electronic submission preparation and review
Review key planning documents to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements
Interact with vendors regarding project standards, programming conventions, programming specifications and file transfers
Provide leadership for ensuring quality of deliverables by consistently applying standards and complying with regulatory requirements
Identify opportunities for increased efficiency and consistency within team and interactions with strategic vendors
Independently lead and perform programming assignments with minimal supervision
Support improvement initiatives.

Requirements

What you’ll need

Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required
Proficiency in SAS
Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development
Demonstrated proficiency in analytical programming
In-depth understanding of clinical data structure (e.g., CDISC standards) and relational databases
Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21
Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM
Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission
Good understanding of regulatory, industry, and technology standards and requirements
Knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs
Demonstrated ability to work in a team environment with clinical team members.

Benefits

Comp & perks

participation in Parexel’s annual performance-based bonus plan
annual salary review
total rewards incentives