Immunology -Jobs | StepStone

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Project Lead - clinical study

Experis

Charleroi

As Project Leader - clinical study, you are in charge to - Experis * Charleroi * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Management of method validation, assay transfer and sample analysis studies; * Prepares and/or reviews worksheets related to studies; * and training appropriately documented; * Ensures high level documents are signed and acknowledged by personnel involved in the study; * Ensures study binders are up to date; * Follows up on assigned study inventory and sample manifest; * Follows up on deviations ; * Follows up on QC review and ensures it is performed in a timely fashion; * Prepares and/or reviews of data tabulation and study related documents; * ; coordinates with the relevant transversal units (e.g. Data Analysis, QC, Sample Management, QA) to deliver quality data on time; * Submits studies to QA and answers to QA reports; As Project Leader - clinical study, you are in charge to - Experis * Charleroi * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Management of method validation, assay transfer and sample analysis studies; * Prepares and/or reviews worksheets related to studies; * and training appropriately documented; * Ensures high level documents are signed and acknowledged by personnel involved in the study; * Ensures study binders are up to date; * Follows up on assigned study inventory and sample manifest; * Follows up on deviations ; * Follows up on QC review and ensures it is performed in a timely fashion; * Prepares and/or reviews of data tabulation and study related documents; * ; coordinates with the relevant transversal units (e.g. Data Analysis, QC, Sample Management, QA) to deliver quality data on time; * Submits studies to QA and answers to QA reports;
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Principal Scientist - immunology

Experis

Charleroi

As Principal Scientist, you are in charge to - Experis * Charleroi * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Reporte to the Associate Director, Scientific Operations, and working closely with the laboratory personnel, * Work within a team focusing on the characterization of the cellular and humoral immune response, using various types of assays such as flow cytometry (phenotyping, receptor occupancy, phosflow, ICS, etc) ELISPOT, ELISA, and viral neutralization tests, * Overseeing experimental design of flow cytometry, ELISPOT and antibody-based assays through generation of study-specific workplans and supporting documentation, * Overall conduct of studies in different immune-therapeutic areas, acting as primary contact to the client for communication of study progress, * Ensures that timelines and milestones are met and are in line with company objectives, As Principal Scientist, you are in charge to - Experis * Charleroi * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Reporte to the Associate Director, Scientific Operations, and working closely with the laboratory personnel, * Work within a team focusing on the characterization of the cellular and humoral immune response, using various types of assays such as flow cytometry (phenotyping, receptor occupancy, phosflow, ICS, etc) ELISPOT, ELISA, and viral neutralization tests, * Overseeing experimental design of flow cytometry, ELISPOT and antibody-based assays through generation of study-specific workplans and supporting documentation, * Overall conduct of studies in different immune-therapeutic areas, acting as primary contact to the client for communication of study progress, * Ensures that timelines and milestones are met and are in line with company objectives,
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QC Reviewer - GLP

Experis

Charleroi

As QC Reviewer, you are in charge to - Experis * Charleroi * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Perform QC review on experimental paperwork in timely fashion. * Review data (tables, forms, calculations, etc.) and reports, as assigned; * Review data tabulation and study related documents; * to identify root cause and improvement opportunities; * Help in implanting good quality control practices; * Prepare the documentation to be transferred to the archives at study finalization; * Review SOP/CSP; * Complete tasks in compliance with GLPs, driving documents and current procedures; * to deliver quality data on time; * Applies and train personnel on Good Documentation Practices (GDP); * Performs biobanking-related activities (sample reception, tracking and inventory) in compliance with applicable procedures; * Performs other duties as assigned. * Train personnel on QC review, as needed. As QC Reviewer, you are in charge to - Experis * Charleroi * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Perform QC review on experimental paperwork in timely fashion. * Review data (tables, forms, calculations, etc.) and reports, as assigned; * Review data tabulation and study related documents; * to identify root cause and improvement opportunities; * Help in implanting good quality control practices; * Prepare the documentation to be transferred to the archives at study finalization; * Review SOP/CSP; * Complete tasks in compliance with GLPs, driving documents and current procedures; * to deliver quality data on time; * Applies and train personnel on Good Documentation Practices (GDP); * Performs biobanking-related activities (sample reception, tracking and inventory) in compliance with applicable procedures; * Performs other duties as assigned. * Train personnel on QC review, as needed.
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