Sr. Clinical Research Associate - Belgium (French & Dutch Fluency)
Core
Senior Clinical Research Associate responsible for independent site monitoring, management, recruitment, and mentoring of junior CRAs to ensure protocol and regulatory compliance in clinical trials.
Role type
Senior IC Clinical Research Associate
Builds
Clinical study execution and data integrity for pharmaceutical/biotech sponsors
Domain
Clinical Research / Life Sciences
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
ICH-GCP compliance, clinical site monitoring, data query resolution, clinical supply coordination, site initiation/qualification, patient recruitment support, TMF management, CRA mentoring
Preferred skills
Sr.CRA or ACRP certification, Phase I-IV trial experience, Health Sciences/Life Sciences/Pharmacy/Nursing degree
Technologies
Medidata Rave, Oracle InForm, eTMF, CTMS, Microsoft Office Suite
Responsibilities
Conduct onsite and remote site monitoring and close-out visits; review source documents for data consistency; coordinate shipment of investigational products and supplies; mentor CRA I and II staff; participate in audits and inspections; support site recruitment and activation; translate site documents when applicable.
Seniority
Senior, hands-on IC