Clinical Research Associate

il y a 1 semaine


Bruxelles, Région de Bruxelles, Belgique Michael Page Temps plein

As a successful Clinical Research Associate (CRA) - Brussels, you will have the following responsibilities:

Study Preparation:

  • Support the design and the development of clinical trial protocols
  • Collect and submit documentation for Board approval
  • Coordinate the preparation of trial- specific training materials

Site Management:

  • Select and monitor clinical trial sites with respect to the sturdy protocol and regulatory requirements
  • Ensure follow-up with the clinical trial sites from A to Z : from site selection to close-out studies

Data Management:

  • Review the accuracy and the completeness of case reports forms, documentation, activities and data
  • Identify, follow-up and resolve data discrepancies

Compliance and Safety:

  • Ensure compliance to regulatory guidelines
  • Monitor, reports and follow-up any adverse events with respect to the regulatory requirements
  • Conduct risk assessments and propose corrective and preventive actions if needed

As a successful Clinical Research Associate (CRA) - Brussels, you have the following requirements:

  • Master Degree in Life Sciences, pharmacy or related fields
  • +2 years of experiences as a Clinical Research Associate (CRA) in the pharmaceutical, biotechnology or CRO industry
  • Experiences in phase I-IV studies
  • Knowledge in regulatory requirements: FDA ...
  • Strong organizational and time management skills
  • Excellent attention for details
  • Strong written and verbal communication skills
  • Fluent in English, French and/or Dutch being a plus

As a successful Clinical Research Associate (CRA) - Brussels, you will have:

  • A competitive salary including a package of extra legal benefits
  • The chance to join a stable company proposing growing possibilities
  • The possibility to join a multicultural supportive team with a nice team spirit

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