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  • Markham, Ontario, Canada Everest Clinical Research Services Inc. Full time $63,453 - $68,500

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  • Markham, Ontario, Canada Everest Clinical Research Services Inc. Full time $63,453 - $68,500

    Job Title: Statistical ProgrammerWe are seeking a highly skilled Statistical Programmer to join our team at Everest Clinical Research Services Inc.Job Summary:The successful candidate will be responsible for processing and validating data and statistical output reports of trial data based on statistical analysis plans and statistical TLGs mock-up shells...


  • Markham, Ontario, Canada Everest Clinical Research Services Inc Full time

    Job Title: Statistical ProgrammerJob Summary:We are seeking a highly skilled Statistical Programmer to join our team at Everest Clinical Research Services Inc. As a Statistical Programmer, you will be responsible for compiling and reviewing SDTM and ADaM dataset specifications, annotated patient Case Report Forms, and other related programming documentation...


  • Markham, Ontario, Canada Everest Clinical Research Services Inc Full time

    Job Title: Statistical ProgrammerJob Summary:We are seeking a highly skilled Statistical Programmer to join our team at Everest Clinical Research Services Inc. As a Statistical Programmer, you will be responsible for compiling and reviewing SDTM and ADaM dataset specifications, annotated patient Case Report Forms, and other related programming documentation...


  • Markham, Ontario, Canada Everest Clinical Research Services Inc Full time

    Job Summary:We are seeking a highly skilled Statistical Programmer to join our team at Everest Clinical Research Services Inc. As a Statistical Programmer, you will be responsible for compiling and reviewing SDTM and ADaM dataset specifications, annotated patient Case Report Forms, and other related programming documentation.Key Responsibilities:Process SDTM...


  • Markham, Ontario, Canada Everest Clinical Research Services Inc. Full time $63,453 - $68,500

    Job Title: Statistical ProgrammerWe are seeking a highly skilled Statistical Programmer to join our team at Everest Clinical Research Services Inc. in Markham, Ontario.Job Summary:The successful candidate will be responsible for compiling and reviewing SDTM and ADaM dataset specifications, annotated patient Case Report Forms (aCRF), and other related...


  • Markham, Ontario, Canada Everest Clinical Research Services Inc. Full time $63,453 - $68,500

    Job Title: Statistical ProgrammerWe are seeking a highly skilled Statistical Programmer to join our team at Everest Clinical Research Services Inc. in Markham, Ontario.Job Summary:The successful candidate will be responsible for compiling and reviewing SDTM and ADaM dataset specifications, annotated patient Case Report Forms (aCRF), and other related...


  • Markham, Ontario, Canada Everest Clinical Research Services Inc. Full time

    Job Title: Statistical ProgrammerEverest Clinical Research Services Inc. is seeking a highly skilled Statistical Programmer to join our team.Job Summary:We are looking for a detail-oriented and analytical individual to work on clinical trial data analysis and reporting. The successful candidate will have a strong background in statistical programming and...

Statistical Programmer

2 months ago


Markham, Ontario, Canada Everest Clinical Research Services Inc Full time
Job Summary

We are seeking a highly skilled Statistical Programmer to join our team at Everest Clinical Research Services Inc. As a Statistical Programmer, you will play a critical role in the development and implementation of clinical trial data analysis and reporting.

Key Responsibilities
  • Compile and review dataset specifications, annotated patient Case Report Forms, and other related programming documentation for integration in reports based on company standard operating procedures and Working Instructions.
  • Process SDTM and ADaM datasets following authorized dataset specifications, including datasets for Clinical Study Reports, clinical trial efficacy and safety data integrations, and other data analysis and reporting needs.
  • Process and validate data and statistical output reports of trial data based on statistical analysis plans and statistical TLGs mock-up shells through developing SAS programming codes.
  • Conduct basic analysis of trends in clinical trial data through developing SAS programming codes for database logical checks and reports for ongoing data review.
  • Collect and consolidate data and programming information from various sources in accordance with company SOPs and WIs to prepare reports to achieve audit readiness during and at the end of the clinical trials for internal and external quality and compliance audits.
  • Achieve a high rating for each of the defined company and trial Sponsor-specific statistical programming Key Performance Indicators (KPIs).
  • Collect, track, and archive clinical trial data (SDTM and ADaM datasets) and programming information in accordance with company archival SOPs and Working Instructions.
  • Maintain current knowledge of pharmaceutical clinical research industry standards, conventions, and regulatory requirements, as well as the knowledge of clinical trial Sponsor-specific requirements when applicable.
  • Comply to company-specific and clinical trial Sponsor-specific training requirements.
  • Develop and provide expertise in other programming and system administration areas when required.
  • May lead statistical research efforts for assigned projects.
  • May participate in the development and maintenance of clinical trial data and statistical reporting standards to ensure that the company standards are up to date and in line with pharmaceutical industry standards, conventions, and regulatory requirements.
  • Provide technical guidance and support to less experienced Statistical Programmers in the study teams.
  • May make decisions on time allocation to complete assigned projects.
  • May make decisions on therapeutic area programming standards/conventions/procedures within assigned therapeutic areas as a lead programmer.
  • May make decisions on client-specific programming standards/conventions/procedures for assigned clients when required.
  • May make decisions related to setting project priorities, resource availability, negotiation of project timelines, on therapeutic area and client-specific programming standards/conventions/procedures, and on client-specific programming.
Requirements
  • Master's degree in statistics, biostatistics, epidemiology, bioinformatics, mathematic, or computer sciences.
  • 1-3 years of experience in clinical trial statistical programming and/or data analysis.
  • Advanced level proficiency in SAS.
  • Demonstrated strong capabilities and/or sustained high level of performance as a Statistical Programmer.
  • Experience with the following is required: Microsoft Word, Excel, PowerPoint, Outlook, Project.
  • Experience with statistical software is preferred.
  • Must be action-oriented, have composure, be creative, be customer-focused, have functional and technical skills, able to learn on the fly, able to persevere, excellent planning, organizational, time management, and problem-solving skills, able to prioritize, and able to pick up on new technical skills quickly.