Title: Senior Clinical Research Associate
Location: Belgium (remote)
Salary: Up to €82,000 plus car allowance/company car and benefits
My client are a top global CRO specialising in the completion of complex clinical trials are a global leader in delivering comprehensive, integrated drug development services to the pharmaceutical, biotechnology, and medical device industries.
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 4 + years of independent clinical monitoring experience (comparable to CRA I + CRA II), ideally within CRO/pharma.
Valid driver’s license and right to work in Belgium
Strong knowledge of ICH‑GCP, EU/FDA regulations, local Belgian requirements
Benefits
Competitive salary with company car or car allowance
Private healthcare
Financial assistance with home office setup
Ability to purchase extra holiday in addition to 30 days holiday
Please apply via LinkedIn or contact myself at chris.boateng@arm.co.uk