You will be responsible for the implementation and end-to-end operational execution of each GCO clinical study strategy as it relates to selected biospecimens samples
Job Summary
You will be responsible for the implementation and end-to-end operational execution of each GCO clinical study strategy as it relates to selected biospecimens samples.
Contribute to providing input on clinical sample assessment sections in clinical trial-related documents and create study-specific sample collection tables.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
Matching Summary
You will be responsible for the implementation and end-to-end operational execution of each GCO clinical study strategy as it relates to selected biospecimens samples.
Skills & Requirements
Must-have
Human sample management
Clinical sample assessment input
Central lab systems experience
Kit design and protocol contribution
Biospecimen collection timepoints
Nice-to-have
Cross-departmental communication
Ethical considerations for biospecimens
Risk management and escalation
Key Requirements
Previous CRO or vendor experience
Human sample management experience
Understanding of clinical sample assessments
Lab design from trial protocol perspective
Central lab systems and data transfer specifications experience
Science degree
Lab background in sample management and processing