[Hiring] Statistical Programmer I @Everest Clinical Research

Role Description

We are seeking committed, skilled, and customer-focused individuals to join our winning team as a Statistical Programmer I at our Markham, Ontario on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.

Accountabilities:

• Statistical Programming:
  • Under supervision, develop and review SDTM and ADaM dataset specifications, annotated Case Report Forms (CRF), and other related documents based on Statistical Analysis Plan (SAP), Everest company Standard Operating Procedures (SOPs), and industry data standards.
  • Program and validate SDTM and ADaM datasets following approved specifications; perform CDISC conformance checks and address findings.
  • Develop SAS programs to generate and validate statistical output reports of trial data based on the SAP and TLGs mock-up shells.
  • Provide statistical programming support to Clinical Study Reports and other data analysis needs such as regulatory required safety reports and exploratory data analyses.
• Clinical Data Acquisition and Cleaning Support:
  • Develop and maintain SAS programs for database integrity checks and work with Data Managers to address data issues.
  • Support data acquisition of non-CRF data by developing SAS programs to reconcile CRF and non-CRF data.
  • Generate data listings, summary tables, and graphs for ongoing data cleaning and scientific data surveillance reviews.
  • Develop SAS programs to generate Patient Profiles for trial subject case review activities.
  • Document data and programming information in accordance with Everest company SOPs and WIs.
  • Achieve a high rating for defined Everest company and trial Sponsor-specific statistical programming key performance indicators.
  • Maintain current knowledge of pharmaceutical clinical research industry standards and regulatory requirements.
  • Comply with Everest company-specific and clinical trial Sponsor-specific training requirements.
  • Provide expertise in other programming and system administration areas when required.

Qualifications

• A Master’s or Ph.D. Degree in statistics, biostatistics, epidemiology, public health, bioinformatics, mathematics, or computer sciences.
• SAS certified Base/Advanced.
• Clinical trials programmers are highly preferred; exposure/experience in clinical trial statistical programming and/or data analysis is desirable.

Requirements

• Master’s or Ph.D. Degree in relevant fields.
• SAS certified Base/Advanced.
• Experience in clinical trial statistical programming and/or data analysis is desirable.

Benefits

• Medical, dental, and vision coverage.
• Life & AD&D insurance.
• Short- and long-term disability.
• Tuition reimbursement.
• Fitness reimbursement.
• Employee assistance program (EAP).
• Pension plan.
• Generous paid time off and sick leave.
• Opportunity to earn a performance-based bonus.
• Estimated Salary Range: $45,000 - $55,000.