Senior Clinical Data Coordinator: Oncology Trials & QA

IQVIA; Manchester; On-site; GBP 40,000 - 60,000; Full time

Job summary

IQVIA in Manchester seeks a Senior Clinical Data Coordinator to conduct data review, UAT, and QC for Phase I–III trials in line with ICH/GCP standards.

The role requires 3+ years in data management, EDC experience (Oracle Inform preferred) and oncology/inflammatory experience. Not eligible for UK visa sponsorship. IQVIA provides global clinical research services and healthcare intelligence.

Qualifications

• Minimum of 3 years of data management experience.
• Experience with Electronic Data Capture (EDC) systems, Oracle Inform preferred.
• Oncology and/or inflammatory therapeutic area experience.
• Bachelor's degree or allied health certification preferred.

Responsibilities

• Perform ongoing data review, including reconciliation of third-party data streams and serious adverse event reconciliation with the safety database.
• Perform User Acceptance Testing (UAT) of clinical databases.
• Perform Quality Control (QC) of clinical databases.
• Perform ongoing updates of Data Management-related documentation, as needed.

Skills

Data management

Attention to detail

Problem solving

Education

Bachelor's degree or allied health certification

Tools

Oracle Inform EDC

Job description

IQVIA in Manchester seeks a Senior Clinical Data Coordinator to conduct data review, UAT, and QC for Phase I–III trials in line with ICH/GCP standards.

The role requires 3+ years in data management, EDC experience (Oracle Inform preferred) and oncology/inflammatory experience. Not eligible for UK visa sponsorship. IQVIA provides global clinical research services and healthcare intelligence.