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
Solliciteren