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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

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