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Project Lead

What are your responsibilities?

As Project Leader - clinical study, you are in charge to

  • Management of method validation, assay transfer and sample analysis studies;
  • Prepares and/or reviews worksheets related to studies;
  • Ensures personnel are trained 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;
  • Works in collaboration with the Principal Scientists, the Research Assistants and the Research Associates; 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;
  • Schedules experiments based on the timelines, priorities and requirements;
  • Writes and reviews method SOP/CSP;
  • Performs biobanking-related activities (sample reception, tracking and inventory) in compliance with applicable procedures;
  • Performs other duties as assigned;
  • Responsible for coaching, mentoring, training and day to day interaction with the Research Assistants and the Research Associates for assigned studies.

Levels, Fashion, Producing, Soft Skill, Data analysis, Clinical Research, Coaching, Protocols, SOP, Life Science, Containment, Immunology, Data Quality, Mentoring, Health & Safety, Validation, Scheduling, Research, HIV, GLP, CSP, Health & Safety, VOS, Reception, Biosafety, Sample Management, Quality Control, Management, Organization Skills, Viruses, Analysis, Coaching, Biotechnology, Quality assurance, Cross Functional

Project Lead

Experis, Charleroi
Categories: 
Quality / Security / Environment, IT, Developer, C# Developer
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