Contract Non-Clinical Statistician job in Brussels

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This vacancy has now expired. Please see similar roles below...

A top 10 global pharmaceutical company is currently recruiting a Contract Non-Clinical Statistician. This organisation develops innovative products across multiple therapy areas including cardiovascular, oncology, and respiratory, and employs 100,000 staff globally. Based in the company's office in Belgium, this position offers an exciting opportunity to work with an internationally renowned company and bolster a career in the clinical field.

Job Responsibilities:

Performing Six sigma analysis to assess process performance.
Designing experiments to assess the effect of controlled factors on process.
Performing multivariate analyses for process/method understanding and optimization.
Performing measurement system analysis, tolerance intervals, and stability data analysis to understand.
Main sources of process/method variation/noise.
Statistical process control, breakpoint analysis for process/method control.
Validating and transferring analytical methods to assess and/or improve product quality and process robustness.
Writing statistical presentations/reports of performed studies within a GMP compliant environment in alignment with current ICH / FDA guidelines and GSK SOPs.
Acting as a major contributor to provide statistical guidance and methodology for one or more project teams, investigations, and/or trouble shooting.
Reporting results and conclusions back to project teams and stakeholders.
Supporting, training, and coaching less experienced statisticians in the group and organization.
Supporting the improvement of data collection process to enable quick and reliable data analysis and improving quality of data (data integrity); interacting with Manufacturing sites and QCs to align data evaluation methods.
Contributing to the development of new statistical approaches and automatized tools to provide statistical evaluation.
Participating actively in the GIO/QC statistical community and functional teams aiming at exchanging best practices and view amongst experts.

Skills and Requirements:

Master's Degree in (Bio)Statistics or scientific background with relevant statistical background.
Experience as a statistician in the field of pharmaceutical statistics, with experience in manufacturing and/or quality control (QC) operations.
Experience in statistics applied to biological manufacturing processes and/or QC tests.
Knowledge of pharmaceutical regulatory environment, ICH and USP guidelines.
Demonstrable multitasking, project management, and execution skills.
Good interpersonal skills, including communication, presentation, persuasion, and influence.
Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Emma Adams at +44 203 854 3893 or upload your CV on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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