Clinical Data Coordinator

Key Responsibilities: Support day to day clinical data management activities across assigned studies, ensuring data is accurate, complete and compliant throughout the study lifecycle. Perform data review and cleaning, generating, issuing and resolving queries with sites in line with the Data Management Plan and study timelines. Assist with database setup and user acceptance testing (UAT), including review of CRF/eCRF designs, edit check specifications and completion guidelines. Reconcile external and third-party vendor data (e.g. lab, ECG, IRT) and SAE data against the clinical database. Maintain study documentation and Trial Master File records, ensuring all work follows SOPs, GCP and regulatory requirements. Track and report data management metrics, communicating progress, issues and risks to the Clinical Data Manager and wider study team. Support interim analyses, database lock activities, and client audits or inspections as needed.

Qualifications & Skills: Bachelor’s degree in life sciences, health sciences, pharmacy or a related field 1+ years of clinical data management or clinical data coordination experience within pharmaceutical, biotech or CRO settings CRO experience (required) Hands-on experience with EDC systems such as Medidata Rave, Veeva Vault CDMS, Oracle InForm or similar Working knowledge of GCP, ICH guidelines and CDISC/CDASH standards Strong attention to detail, organization and the ability to manage multiple studies and deadlines