Clinical SAS Programmer

3 weeks ago

Ottawa, Ontario, Canada Adecco Canada Full time
Job Title: Clinical SAS Programmer

Adecco Canada is seeking a highly skilled Clinical SAS Programmer to join their team in Ottawa. This is a one-year contract role based onsite in Ottawa, Monday-Friday 8am-5pm.

Responsibilities:
  • Generate and validate tables, listings, and figures (TLF) based on specifications provided by Statistics and/or Clinical Writers.
  • Perform all data analytics activities for assigned studies with minimal manager oversight.
  • Ensure that all data analytics activities for assigned studies are completed on time and with high quality or escalate as appropriate.
  • Support EDC development and visualization tools (PowerBI).
  • Communicate well with peers, study teams, and management as appropriate to support studies and goals.
  • Represent the Data Analytics group at study team meetings.
  • Apply best practices and established standards.
  • Have a general understanding of the clinical trial process and regulations that apply.
  • Seek continuing education on the latest in clinical and data science.
  • Follow departmental Standard Operating Procedures (SOPs), and guidelines.
  • Train and mentor junior staff.
  • Additional study-specific activities.
Requirements:
  • Must be eligible to work and reside within Canada.
  • Bachelor's Degree in Data Science, Computer Science, Statistics, Bioinformatics, or a related discipline.
  • Minimum 3-5 years of experience in a programming role.
  • 6-8 years of clinical SAS programming experience, specifically in TLF generation and macro validation.
  • Experience as a clinical SAS programmer, either directly with a sponsor company or a CRO.
  • Minimum **Base SAS certification** (Advanced SAS certification is preferable).
  • Hands-on experience in **R programming**.
  • Experience developing SAS/R programs to generate and validate statistical output reports based on SAP and TLF mock-up shells.
  • Experience generating outputs for regulatory submissions (FDA, Health Canada).
  • Programming experience in R, SQL, and JSON.
  • Provide statistical programming support for Clinical Study Reports, data analysis, and reporting.
  • Develop SAS/R programs to generate data listings, summary tables, and graphs for ongoing data cleaning and scientific data surveillance reviews.
  • Experience with CDISC and SDTM implementation is desirable.
  • Support the development of technical programming specifications for SDTM, ADS, or ADaM standards.
  • Knowledge of EDC development and visualization tools (PowerBI, Tableau) is an asset.
  • Excellent communication skills, both oral and written.
  • Strong analytical skills, creativity, and innovative problem-solving approach.
  • Ability to collaborate effectively with multidisciplinary team members and work independently.
  • Propensity for continuous learning and experimentation.
  • Demonstrated initiative, critical thinking, and problem-solving skills.

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