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 07712412095 or send an up to date copy of your CV to Lynsey@entrustrs.com