Senior Statistician

  • Location
    Ottawa, Ontario
  • Job type
  • Category
    Science - Research

Adecco is currently hiring a full-time Senior Statistician for our Medical Manufacturing client in Ottawa West. This is a 1-year contract opportunity offering full time hours, Monday to Friday. The salary for this position will be determined based on education and experience.

To qualify for this role you much have 10+ years in related work experience developing protocol methodology and statistical analysis plans.

Senior Statistician Responsibilities:

  • In this role you will support the statistical analysis of clinical studies, verification's and validations. ?
  • Responsible for statistical methods sections and statistical analyses in clinical protocols and reports.
  • Ensures accuracy of report text and consistency between summary tables in the body of reports and the corresponding statistical tables and listings.
  • Identifies and corrects common flaws in interpretation of results, inconsistency in presentation or inference to Abbott report guidelines.
  • Works collaboratively with peers to develop quality protocols, CRF, schema, and reports per agreed timelines.
  • Provides accurate and timely answers to questions from clients and others.
  • Communicates basic statistical concepts to other scientists and nonscientists and acts as Subject Matter Expert for the group.
  • Effectively mentors’ non-statistical peers with regard to basic statistical methodology
  • May be responsible for providing or reviewing statistical input for verification and validation studies.
  • Safeguard the environment and facilitate a healthy workplace culture.
  • Other miscellaneous duties as may be required.
  • Senior Statistician Requirements:

  • Undergraduate university Degree (4 year program), or equivalent experience (Engineering, Science or Math with a specialty in Statistics or Biostatistics)
  • 10+ years related work experience developing protocol methodology and statistical analysis plans 
  • The ability to develop appropriate design and statistical methodology to support regulatory submissions for medical devices
  • Advanced Knowledge of: MS Office, SAS JMP, Minitab (or equivalent statistical software)
  • Knowledge of Current Good Manufacturing Practice 21 CFR Part 820 - asset
  • Knowledge of FDA 510K Clearance Guidelines and Best Practices - asset
  • If you are interested in the position of SeniorStatistician in Ottawa, please click “APPLY NOW”.

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    Reference number CA_EN_1_021956_1436772

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