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?

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.

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.

Profile 
  • 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

Recruitbelgium@valesta.com

 

Application form : Junior Clinical Research Professional

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