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CRA

27/02/2019
- Leuven

Job content

As a Clinical Research Associate, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup (if applicable)
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions
Profile

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Experience of 2 years independent on-site monitoring in Belgium
  • Experience in all types of monitoring visits in Phase II and/or III
  • Full working proficiency in English, Dutch and French
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel
  • Valid driver’s license
Contact

For more information, contact Marieke Franken +32 16 30 95 09 or marieke@arcq.be

Contact

Marieke Franken +32 16 30 95 09