Senior Clinical Research Associate - Sponsor Dedicated (Home Based)

About the role

iQVIA is looking for a Senior Clinical Research Associate to join its Sponsor dedicated model in Belgium, working from home. In this model, the team supports the pipelines of a specific sponsor, so the CRA acts as an indication and molecule expert. The role involves site monitoring, recruitment tracking and study documentation, and is open to candidates who can start before December 2026; a discretionary sign-on bonus of up to 4,300 EUR may be offered depending on role level and experience.

Key responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) according to the contracted scope of work and GCP and ICH requirements.
• Work with sites to adapt, drive and track the subject recruitment plan, and administer protocol and study training to sites.
• Evaluate the quality of site practices and escalate quality issues; ensure site documents are available for the Trial Master File and that the Investigator's Site File is maintained correctly.
• Track regulatory submissions, recruitment, CRF completion and data queries, and generate follow-up letters and visit reports.
• Liaise with the study team and, where applicable, support the development of the site-level recruitment plan.

Required profile

• University degree in a scientific discipline or health care.
• At least 3 years of independent, on-site monitoring experience as a CRA in a CRO or pharmaceutical environment.
• Excellent written and spoken Dutch, French and English.
• Good knowledge of GCP and ICH guidelines, and strong organisational and problem-solving skills.

What we offer

• Career development, training and advancement opportunities.
• Flexibility to balance professional and personal commitments.
• Company car, mobile phone and a rewards and benefits package.