Junior Clinical Research Professional

For the moment we have several junior positions within the Pharmaceutical Industry.

  • Do you have a Bachelor or Master degree in the 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?

--> We have several junior postions: CTA, Regulatory Affairs assistant, junior QA officer, ....

Then don’t hesitate and find out more about your career possibilities in the Life Sciences!


Job Description 

As a Junior Clinical Research Professional you are part of a clinical trial team and are responsible for the smooth execution of the clinical trial process. You have a wide variety of tasks and responsibilities.


We currently have several opportunities to start your career in Clinical Research:

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 Assistant

  • 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

Clinical Research Associate

  • You perform monitoring visits from initiation to close out
  • You may support in operational feasibility to assess feasibility of trial in Belgium
  • You ensure detailed corresponding reports and administration
  • You train your investigational site staff on study specific procedures
  • You evaluate appropriate site compliance and data quality
  • You respond to site-related queries and escalate site-related issues
  • You are responsible for operational site management
  • You actively contribute to results oriented department goals

Quality Assurance Assistant

  • You provide support in the development and the implementation of the QA program
  • You participate to the preparation of and during regulatory inspections
  • You take in charge the handling and the follow-up of Quality Complaints
  • You provide support in the department with change control, document control, calibration and deviation follow-up
  • You format, review contents and upload quality documents in the system
  • You organize and follow up on the required trainings

Next to these positions, we occasionally have opportunities as Regulatory affairs assistant, Junior MSL or in the department of Drug Safety.

  • 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 
  • Experience is a plus
Contact Information 

+32 15 21 11 04



Application form : Junior Clinical Research Professional

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