QC & Data Analyst

What You'll Be Doing: Review study charts against SOPs, GCP, GDP and study protocols Enter and verify data within CRF/eCRF systems Perform source-to-CRF/eCRF reconciliation Raise and resolve data queries Support sponsor monitor visits and query resolution Attend Site Initiation Visits (SIVs) Identify data trends and support QC reporting Work closely with CRCs, investigators, sponsors and CRO teams Support onboarding, training and process improvement What We're Looking For 1-3+ years' experience in clinical or biological research Bachelor's degree or equivalent experience Understanding of GCP and clinical research processes Experience with clinical data, source documentation, CRFs/eCRFs or QC Strong Excel, Word and Outlook skills Excellent attention to detail and organisation Strong communication and problem-solving skills Comfortable working independently in a fast-paced clinical research environment

The Opportunity: Join a growing research environment with exposure to a broad range of clinical trials and the opportunity to develop your career across clinical operations, quality and data management.