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Ervaren Monitor Klinische Studies

Location: Zaventem, Belgium

Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors. As a Clinical Research Associate within our full-service model, you’ll have the opportunity to embrace your passion for a specific therapeutic area and work with cutting-edge technology developed specifically for CRAs by CRAs. With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.

  • Full Time
  • Level: Entry-level, Mid-level, Senior-level
  • Travel: Yes

Success profile

What makes CRAs aligned to our full-service model successful? Check out the top traits we're looking for and see if you have the right mix.


Explore this
career path

As you grow your CRA career at IQVIA, you’ll play an important role in helping our customers drive healthcare forward and impact the lives of patients around the world.

  1. CRA 1
  2. CRA 2
  3. Senior
    CRA 1
  4. Senior
    CRA 2
  5. Senior
    CRA 3


Lauren Heffron

“IQVIA empowers you to drive your own path within the organization. As no person’s route is the same and the clinical research landscape is forever changing, you are encouraged to continually seek career growth opportunities and to align your interests with your career goals.”

Lauren, Senior Clinical Research Associate 2

“I really enjoy the diversity of teams and clients the CRA role provides, in addition to the ability to speak with so many different key opinion leaders across the country. Progressing through to a Senior CRA, and now acting as Lead CRA for one of our largest gastroenterology studies, I'm excited at the continued opportunities for success and growth in clinical leadership.”

Joseph, Senior Clinical Research Associate 2

“I work with the most incredible brave minds. We share energy and passion to bring new medicines to the market.”

Carolina, Senior Director, R&D Solutions

What you
can expect

  • Professional Development

    Resources that promote your career growth

  • Work-Life Balance

    Leaders that support flexible work schedules

  • Best-in-class Training

    Programs to help you build your therapeutic knowledge

  • Variety

    Dynamic work environments that expose you to new experiences

  • Growth Potential

    Clear pathways to success

  • Therapeutically Aligned

    Protocols aligned to your expertise

Ervaren Monitor Klinische Studies

Apply now
Location: Zaventem, Brussels-Capital Region, Belgium R1350084

Job description



  • MSc en/of BSc opleidingsniveau.
  • Kennis van Nederlands, Engels en Frans.
  • Goede kennis en toepassing ICH-GCP.
  • Minimaal 2 jaar ervaring als CRA.
  • Ervaring in het gebruik van CTMS, eTMF en EDC systemen.
  • Ervaring in verschillende studies, fases, visites en therapeutische indicaties.
  • Passie voor wetenschap, helpen van patiënten en samenwerken met de sites.


  • Uitvoeren van visites (zoals selectie, initiatie, monitoring en close-out) volgens ICH-GCP richtlijnen.
  • Begeleiding van junior CRAs.
  • Ondersteuning van de site(s) i.v.m. patiëntenwerving.
  • RCA en CAPA management.
  • Rapportering van visites en voortgang van de studies.
  • Beheer en archivering van studie-documenten in eTMF.
  • Samenwerking met het project-/studie team.
  • Documentatie in Monitoring Visit Reports en follow-up brieven.



IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at

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