Sr. Clinical Research Associate - Belgium (French & Dutch Fluency)

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in the execution of clinical study plans. Provides guidance and mentoring CRA I and II, collaborating effectively with cross-functional stakeholders in a dynamic, results-driven and high-accountability environment. Perform CRA Assessment Visits and participate in audits/inspections, when required.

Site Monitoring activities (55-60%)

Site Management activities (15-20%)

Site Recruitment and Setup (15-20%)

Mentoring and Internal Initiatives (5-10%)

QUALIFICATIONS

ADDITIONAL KNOWLEDGE / SKILLS

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