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    Quality Training Consultant - London, United Kingdom - ClinChoice

    ClinChoice
    ClinChoice London, United Kingdom

    1 week ago

    ClinChoice background
    Description

    Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture.

    The Principal Biostatistician Consultant is a delivery focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the Programming effort to deliver technical programming and information components of a project.

    Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.
    Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.
    Responsible for assuring that data for statistical analyses are complete, accurate and consistent.
    Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.
    Responsible for validity of analysis and explore alternative analysis strategies as needed.
    Recognizes and corrects flaws in scientific reasoning and statistical interpretation.

    Responsible for accuracy and consistency of statistical tables, figures, and data listings, accuracy of report text, and consistency between summary tables in the body of reports and the corresponding source tables and listings.

    Identifies and corrects common flaws in interpretation of results, inconsistency in presentation or inference, adherence to the report guidelines, and assures project-wide consistency.

    Effectively mentor peers with regards to statistical methodology and provide appropriate training to less experienced statisticians.

    Manage activities of statisticians across projects by appropriately coordinating assignments and reviewing work so that projects are delivered on time with high quality.

    MS or PhD in Statistics, Biostatistics or related field. PhD with 3-5 years of experience or MS with 6-8 years of experience.
    Pharmaceutical, CRO, or related industry experience with clinical trials, including interaction with Regulatory Agencies, especially FDA.

    If you have the requirements we need, you will be invited for phone interview as the first step.

    ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

    We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.


    Our mission drives our culture:

    to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

    Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel.

    The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.

    We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity.
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