Associate Director of Project Management Services

3 weeks ago

Mississauga, Canada GlaxoSmithKline Full time
strong>Nom du site: Mississauga Milverton Drive
Date de publication: Oct 1 2024
Clinical Operations Planning & Feasibility Associate Director

As R&D efforts follow science without constraint, we need to take full advantage of our internal data and expertise, as well as leverage external services and technology, to inform, optimize and validate our clinical trial protocols and study delivery plans. This includes the management of a robust site feasibility process.

As such we are seeking to appoint a Clinical Operations Planning & Feasibility Associate Director to create data driven, high quality insights and modelling to support clinical operations project and study team members. This role will directly support clinical operations planning activities.

Key Responsibilities include, but are not limited to:
  1. Use internal and industry data sources, along with data analytics, to generate insights used for the planning of clinical trials.
  2. Utilisation of current and emerging data sources to identify risks and challenges to optimise clinical trial protocol design.
  3. Lead the site feasibility process in close partnership with the network of local country teams.
  4. Provide timely, high-quality deliverables (e.g. recruitment plans, feasibility country pre-selection and final selection recommendations, etc.) li>
  5. May support the assessment, piloting and embedding of new data analytics and data sources to ensure GSK continues to access best in class solutions.
Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  1. Bachelor’s degree in relevant field.
  2. Excellent project management skills gained in a complex matrix organization.
  3. Results orientated with a drive to set and reach challenging goals with high standards for performance.
  4. Ability to analyse data from divergent sources and translate it into meaningful recommendations.
    1. Knowledge of Agile methodology.
    2. Experience utilizing industry clinical trial related data sources (i.e., li>
    3. Experience with data manipulation, visualization, or advanced analytics.
    4. High level of proficiency with Microsoft Office.

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