Senior Biostatistician

2 months ago

Toronto, Ontario, Canada Everest Clinical Research Services Inc Full time
About Us

Everest Clinical Research Services Inc is a leading contract research organization (CRO) providing comprehensive clinical research services to the pharmaceutical, biotechnology, and medical device industries.

Job Summary

We are seeking a highly skilled Senior Biostatistician to join our team in Markham, Ontario or remotely from a home-based office in Canada. The successful candidate will lead efforts in resolving day-to-day work-related issues and problems, securing quality, improving efficiency and productivity of statistical and programming operations.

Key Responsibilities
  1. Leadership and Project Management:
  • Lead assigned projects by applying project management skills, statistical and programming techniques; achieve quality and on-time delivery of deliverables, earn client's trust and repeat business.
  • Provide statistical expertise for design, analysis, and reporting of clinical trials and research projects.
Statistical Planning and Methodologies:
  • Contribute to the writing of statistical sections of study protocols, perform sample size calculation, develop randomization specifications, and generate randomization codes.
  • Write Statistical Analysis Plans (SAPs) and properly address Peer Statistician review comments.
  • Create and maintain Statistical and Programming Quality Control (QC) and QA Plans for assigned projects.
  • Provide input to unblinded data management plan when required.
  • Assist in research and development of statistical methodologies and processes.
Statistical Programming:
  • Develop and/or review ADaM dataset specifications. Review and provide input to SDTM dataset specifications when required.
  • Perform QC validation of analysis datasets and TLGs.
  • Perform third-level review of dry runs and final run.
  • Lead statistical dry runs and final run by actively participating or contributing to project and resources management, addressing statistical and programming questions and interacting with data management to follow up and resolve data issues.
Statistical Analysis and Reporting, and Publication Support:
  • Perform statistical analysis as per SAP, and address peer/QC review comments and findings.
  • Perform statistical validation of core results, address additional QC validation comments and findings on the core results.
  • Plan and conduct or contribute to the trial results reporting/dissemination meetings.
  • Under supervision contribute to the contents describing any deviation from the planned analysis and deviation from study conduct for the Clinical Study Report (CSR). Review CSR to ensure accuracy, completeness, and appropriateness of the interpretation of the statistical results.
  • Write statistical report or statistical sections of the CSR.
  • Perform statistical analyses for publications, including but not limited to abstracts, manuscripts, presentations, and posters.
Supporting Clinical Data Collection and Cleaning:
  • Provide statistical input to Case Report Forms (CRF) design and database/variable structure.
  • Provide statistical input to non-CRF data collection and acquisition methods and approaches.
  • Review Data Management Plan sections relating to critical data collection and cleaning. Provide statistical input to Data Validation Specification.
  • Specify and/or program database quality acceptance checks, assess and report data quality issues, and follow through until resolution.
  • Perform ongoing assessment and communication of data quality issues, including protocol deviations.
  • Assist data management and trial management team in preparing for database lock.
Requirements

A Ph.D. degree in statistical science, mathematical analysis, or related fields plus 2 years highly relevant experience or a Master's degree plus 4 years highly relevant experience, with demonstrated ability and sustained performance.

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