Title: Clinical Research Associate (FSP)
Location: Netherlands (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 EETINGS 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