Statistician

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

Our client is a diversified health care innovator with a legacy of pioneering work in medical diagnostics and devices. They are dedicated to advancing innovative with-patient diagnostic technology to improve patient care and system efficiency by fundamentally changing the way health care professionals process patients through their system.

Statistician main responsibilities:

  • 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.
  • Communicates basic statistical concepts to other scientists and nonscientists and acts as Subject Matter Expert for the group.
  • Safeguard the environment and facilitate a healthy workplace culture.
  • Other miscellaneous duties as may be required.
  • Statistician Qualifications:

  • Minimum education of bachelor’s degree Engineering, Science or Math with specialty in Statistics or Biostatistics.
  • Minimum experience of Typically requires a minimum of 3 years of related work experience developing protocol methodology and statistical analysis plans or an equivalent combination of education and work experience.
  • Skills of excellent communications skills, both oral and written.
  • Ability to form and develop interpersonal, professional relationships; displays socially and professionally appropriate behavior.
  • Proven ability to demonstrate strong decision-making and problem-solving skills.
  • Ability to influence without authority.
  • The ability to develop appropriate clinical study design and statistical methodology to support regulatory submissions for medical devices.
  • Programming in multiple statistical software (e.g., R; SAS; Minitab; etc.)
  • Knowledge of International Harmonized Committee Good Clinical Practices, IHC/GCP is desirable.
  • Knowledge of FDA 510K Clearance Guidelines and Best Practices is desirable.
  • #A1956

     




    • Apply with Adecco

    Reference number CA_EN_1_027616_1708028

    Accommodation will be provided in all parts of the hiring process as required under Adecco’s Employment Accommodation policy. Applicants will need to make their needs known in advance to their Adecco representative.

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