Clinical Research Associate

Title: Clinical Research Associate (FSP)

Location: Belgium (remote)

Salary: Up to €62,000 plus car allowance/company car and benefits

My client is a top global CRO specialising in the completion of complex clinical trials and is a global leader in delivering comprehensive, integrated drug development services to the pharmaceutical, biotechnology, and medical device industries.

PLEASE NOTE: THIS IS A SINGLE SPONSOR ROLE, MONITORING BETWEEN THE NETHERLANDS/BELGIUM BORDER, WITH A REQUIREMENT TO ATTEND MEETINGS ONCE A MONTH IN BAVRE, BELGIUM.

Responsibilities

• Independently conduct on-site and remote monitoring visits, ensuring protocol, regulatory, and ICH‑GCP compliance, including source data verification (SDV), case report form (CRF) review, and investigational product accountability
• Apply risk-based monitoring approaches, conduct root‑cause analyses, and implement corrective/preventive actions to address site performance issues
• Maintain regular contact with investigative sites between visits to track issue resolution and protocol adherence
• Provide trial status updates to Clinical Team Manager (CTM) and ensure CTMS data is current

Experience

• At least 6 months of independent clinical monitoring experience (comparable to CRA I + CRA II), ideally within CRO/pharma.
• Valid driver’s license and right to work in the Netherlands
• Strong knowledge of ICH‑GCP, EU/FDA regulations and local Belgian requirements
• Fluent in French, Dutch and English

Benefits

• Competitive salary with company car or car allowance
• Private healthcare
• Financial assistance with home office setup
• Ability to purchase an extra holiday in addition to the 30-day holiday