Junior Statistical Programmer - Clinical Trials (SAS)

Cytel

Topeka (KS)

Vor Ort

USD 65.000 - 90.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Cytel is seeking a Recent Graduate Statistical Programmer to join a pharmaceutical client project in the United States. You will develop SAS-based analyses across Phase I–IV trials with a focus on data manipulation, reporting, and ownership of deliverables.

The role emphasizes collaboration in a globally dispersed team, preparing submission-ready datasets and files, and expanding your programming and life sciences knowledge under Cytel guidance.

Qualifikationen

  • Perform data manipulation, analysis and reporting of clinical trial data using SAS.
  • Create and validate datasets, analysis files, tables, listings and figures (TLFs).
  • Generate ad-hoc reports and prepare submission packages.
  • Apply understanding of efficacy analysis and regulatory expectations.
  • Collaborate effectively in a globally dispersed team and meet deadlines.

Aufgaben

  • Perform data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming.
  • Applying your SAS programming skills, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s).
  • Generating ad-hoc reports.
  • Preparing and validating submission packages.
  • Applying your understanding/experience with Efficacy analysis.
  • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
  • Being adaptable and flexible when priorities change.

Kenntnisse

Data manipulation
Data analysis
Reporting
English communication

Ausbildung

Undergraduate study (4+ years)
Graduate-level education (2+ years)

Tools

SAS

Jobbeschreibung

Cytel is seeking a Recent Graduate Statistical Programmer to join a pharmaceutical client project in the United States. You will develop SAS-based analyses across Phase I–IV trials with a focus on data manipulation, reporting, and ownership of deliverables.

The role emphasizes collaboration in a globally dispersed team, preparing submission-ready datasets and files, and expanding your programming and life sciences knowledge under Cytel guidance.

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