We are looking for an experienced CRA / TM (Clinical Research Associate / Trial Monitor)

At Sillar Clinical we are currently looking for experienced CRA / TM (Clinical Research Associate / Trial Monitor).  A CRA / TM is responsible for overseeing the progress of a study and ensures that the study is conducted, recorded and reported in accordance with the GCP/ICH guideline, applicable regulatory requirements and relevant SOPs.

Education and/or Experience

  • Have experience working as a CRA / TM for several years
  • Fully proficient in reading, writing and speaking Dutch, French and English
  • Must be a resident of, or living in, Belgium
  • A minimum bachelor degree in a medical, health or science related area
  • Excellent knowledge of Good Clinical Practice (GCP)
  • Knowledge of local regulatory, ethics and institutional contract procedures and submissions
  • Knowledge of trials in medical devices is considered an asset but not required


  • Must be willing to travel if required.
  • Good problem solving and analytical skills
  • Service orientated approach, flexible and open to change
  • Ability to work unsupervised taking responsibilities for own actions
  • Excellent interpersonal and organisational skills
  • Systematically perform activities in a timely and accurate manner
  • Work precisely according to procedures, rules and regulations

If interested, please contact