Clinical Trials Data Coordinator (Internal)

Wye Valley Nhs Trust; Hereford; On-site; GBP 26,000 - 36,000; Full time

Job summary

Wye Valley NHS Trust is seeking an enthusiastic and organised individual to join our Clinical Trials Team to coordinate data collection, entry, validation and reporting across multiple studies. You will liaise with clinicians, investigators and sponsors to resolve data queries, ensure timely submissions and maintain trial documentation in line with GCP and data protection requirements.

Experience in a clinical environment and good organisational skills are essential.

Qualifications

• Experience of working in a clinical environment.
• Ability to coordinate data collection and reporting.
• Understanding of GCP and data protection requirements.
• Strong organisational skills and attention to detail.

Responsibilities

• Collect, enter, validate and report clinical trial data accurately and within deadlines.
• Identify and resolve data discrepancies, respond to queries and elevate concerns appropriately.
• Coordinate patient assessments, appointments, recruitment and follow-up activities in line with trial protocols.
• Liaise with clinical teams, researchers, sponsors and Clinical Trials Units.
• Maintain trial records, site files, spreadsheets, databases and EDGE recruitment reports.
• Ensure compliance with research protocols, GCP, governance requirements and patient confidentiality.
• Undertake data quality checks, internal audits and support audit readiness.
• Review and improve data collection processes, SOPs and work instructions.
• Provide guidance and training to colleagues on clinical trial data procedures.
• Manage competing priorities, contribute to research promotion and service improvement.

Job description

Wye Valley NHS Trust is seeking an enthusiastic and organised individual to join our Clinical Trials Team to coordinate data collection, entry, validation and reporting across multiple studies. You will liaise with clinicians, investigators and sponsors to resolve data queries, ensure timely submissions and maintain trial documentation in line with GCP and data protection requirements.

Experience in a clinical environment and good organisational skills are essential.