Junior Pharmaceutical Consultant

For several clients, we are looking for enthusiastic Junior Pharmaceutical Consultants: 

  • Do you have a Bachelor, Master or PhD degree in a paramedical area, biomedical or pharmaceutical sciences?
  • Are you fluent in English and do you have good knowledge of Dutch and/or French?
  • Are you meticulous, quality-oriented and possess good communication skills? 

Your career in the Pharmaceutical Industry is waiting for you! 

Job Description 

As a Junior Pharmaceutical Consultant you can start your career in diverse domains (Clinical Research, Production, ...), each one with a wide variety of tasks and responsibilities.


Data Management/ Database Validation

  • Review of electronic case report forms (eCRF’s)
  • Check clinical databases on inconsistent, missing and incorrect data
  • Generate queries towards the sites in order to get the data clean
  • Review functional specifications for database-tools
  • Create test steps and validation documents for User Acceptance Testing
  • Coordinate all trial and sponsor related trainings and oversee that training programs are followed and documented
  • Organize User Acceptance Testing
  • Communications with all involved parties

Clinical Trial Associate

  • Follow-up on clinical trial administration, meeting coordination, minute taking, travel arrangements, faxing, copying and mailing
  • Review of study documents for completeness, consistency and accuracy
  • Completion of relevant Clinical Trial Management System (CTMS) fields, databases, tracking tools, timelines and project study plan
  • Liaison with study sites and establishment of good communication lines with various departments
  • You are the single point of contact between the clinical study team (internal & external) and project manager

Quality Assurance Assistant

  • Administrative support (prepare meetings, correspondence, archiving, ...)
  • Support to QA Manager, Qualified Person and Quality Assurance Officer
  • Preparation of releases and maintain the overview of all releases
  • Support in the repackaging process
  • To handle the reference standard request from the authorities
  • To give support in the artwork process
  • Support in the receipt of scientific questions, adverse events and complaints (backup)
  • Support in the management of returned products
  • Temperature management (data loggers used during transport)
  • Quarterly RIZIV reporting on sequential labeling.
  • Archiving of release samples, artworks,…


  • Bachelor in the paramedical area, Bachelor Medical Management Assistant, Master Biomedical or Pharmaceutical Sciences, Master in Medicine, PhD in a scientific field … 
  • Fluent in English, good knowledge of Dutch and/or French
  • Eye for detail, quality-oriented and well-organized
  • Good communication skills, team player
  • Stress-resistant 
  • a first experience is a plus
Contact Information 
1 Start 2 Complete

Application form : Junior Pharmaceutical Consultant

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Files must be less than 3 MB.
Allowed file types: txt rtf html pdf doc docx odt.

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