An exciting opportunity is available for a proactive and organised Clinical Trial Associate (CTA) to join a growing biotechnology company supporting the delivery of clinical studies from start-up through to close-out.
Key Responsibilities
Support the coordination and delivery of clinical trials in line with ICH-GCP, protocols and SOPs
Maintain study documentation, trackers, CTMS and eTMF systems
Support study start-up activities, vendor coordination and site communications
Assist with meeting coordination, agendas, minutes and action tracking
Support budget tracking, PO/invoice processing and study administration
Contribute to inspection readiness and quality/compliance activities
About You
Previous experience in Clinical Operations, CTA or study coordination within biotech, pharma or CRO environments
Understanding of ICH-GCP and clinical trial processes
Experience using systems such as CTMS, eTMF or EDC
Strong organisational skills with excellent attention to detail
Confident communicator with the ability to manage multiple priorities in a fast-paced environment
What s on Offer
Opportunity to join a growing and innovative biotech environment
Broad exposure across end-to-end clinical trial delivery
Collaborative and supportive culture
Strong development and progression opportunities
Flexible remote working setup
To hear more about this opportunity, please call Lynsey today on (phone number removed) or send an up to date copy of your CV to (url removed)
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