Senior Clinical Statistical Programmer (US/Canada)

Added
less than a minute ago
Type
Full time
Salary
Salary not provided

Related skills

r python sas cdisc adam

๐Ÿ“‹ Description

  • Independently develop and maintain SAS programs for clinical studies (ADaM).
  • Peer QC, double programming and validation of study outputs.
  • Lead statistical programming activities on studies and deliverables.
  • Assist Management and Biostatisticians on complex projects.
  • Design and implement SAS programs for standardized use.
  • Ensure compliance with study protocol and departmental procedures.

๐ŸŽฏ Requirements

  • Bachelor's degree in Statistics, Math, Physics, or Computing related field.
  • Minimum 3 years of hands-on statistical programming in CRO/pharma trials.
  • Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS.
  • Experience applying CDISC for ADaM datasets and docs (define.xml).
  • Familiarity with Pinnacle21 validation.
  • Experience in early-phase clinical trials and PK/PD analysis programming.

๐ŸŽ Benefits

  • Celerion is an equal opportunity employer.
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