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Parexel

Statistical Programmer II – FSP

Parexel

. Provide technical expertise for the conduct of clinical trials .

Posted 9/23/2026full-timeRemote • Poland, Romania, Hungary, SerbiaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in SAS programming for clinical trials, with a strong focus on producing and quality-controlling derived datasets in compliance with CDISC standards. Effective communication and collaboration skills are essential for working in a global environment and supporting client processes.

Highest-signal resume keywords
SAS ProgrammingCDISC StandardsDerived Dataset ProductionQuality ControlStatistical Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
SAS BaseSAS/STATSAS/GRAPHSAS MacrosStatistical TerminologyClinical TestsProtocol Designs
Soft Skills
Attention to DetailWritten CommunicationVerbal Communication
Tools & Technologies
Client Systems
Industry Keywords
Clinical TrialsBiostatisticsRegulatory ComplianceData ListingsKnowledge Sharing

About the role

Key responsibilities & impact
  • Provide technical expertise for the conduct of clinical trials
  • Support programming activities related to the analysis and reporting of clinical study data with minimal supervision
  • Potentially fill the Statistical Programming Lead role, or part of it, on small, non-complex projects
  • Deliver high-quality service using client systems and following client processes
  • Work closely with client teams and Parexel colleagues in a global environment
  • Produce derived datasets, including SDTM and ADaM, tables, figures, and data listings of any complexity
  • Quality-control low-medium complexity derived datasets, tables, figures, and data listings
  • Develop and QC derived dataset specifications and other process-supporting documents
  • Maintain complete traceability and regulatory compliance
  • Participate in and contribute to programming community knowledge-sharing sessions

Requirements

What you’ll need
  • Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences
  • Minimum 3 years of SAS programming experience in clinical research
  • Proficiency in SAS Base, SAS/STAT, SAS/GRAPH, and SAS macros
  • Strong understanding of CDISC standards
  • Knowledge of statistical terminology, clinical tests, and protocol designs
  • Excellent attention to detail with a focus on quality
  • Strong written and verbal English communication skills

Benefits

Comp & perks
  • Fully flexible work arrangement; you can be fully home based
  • Open and friendly work environment
  • Opportunities to develop long-term careers
  • Opportunity to develop within the role and take on further responsibilities
  • Opportunity to develop skill sets within other related departments
  • Long-term job security and prospects