Senior Clinical Data Coordinator: Trials Data & QC

IQVIA Argentina; Manchester; On-site; GBP 40,000 - 55,000; Full time

Job summary

IQVIA is seeking a Senior Clinical Data Coordinator to support Phase I-III trials in accordance with ICH/GCP guidelines. You will oversee data review, reconcile third party data streams and serious adverse events with the safety database, and perform UAT and QC on clinical databases.

Ideal candidates hold a Bachelor's degree or related allied health certification with at least 3 years of data management experience, plus experience with EDC systems (Inform preferred).

Qualifications

• Bachelor's degree or related allied health certification required or commensurate experience.
• Minimum of 3 years data management experience.
• Experience with EDC systems required; Inform EDC preferred.
• Oncology and/or inflammatory therapeutic area experience beneficial.

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 experience

Oncology experience

Education

Bachelor's degree or related allied health certification

Tools

Inform EDC

Job description

IQVIA is seeking a Senior Clinical Data Coordinator to support Phase I-III trials in accordance with ICH/GCP guidelines. You will oversee data review, reconcile third party data streams and serious adverse events with the safety database, and perform UAT and QC on clinical databases.

Ideal candidates hold a Bachelor's degree or related allied health certification with at least 3 years of data management experience, plus experience with EDC systems (Inform preferred).