Clinical Data Coordinator II

Overview

As a Clinical Data Coordinator II specializing in clinical trials within a study team, you will be contributing to the study to ensure all tasks are completed within a timely manner. You will be taking responsibility for data management aspects of study deliverables within reporting teams for non‑complex deliveries.

Responsibilities

• Data review using SAS listings & Excel, including SAE reconciliations and coded data listings
• Database testing within Medidata Rave, reviewing edit check outputs and actioning as appropriate
• Reviewing draft documents for third party data, updating documents and reviewing reconciliation outputs
• Production of status reports

Qualifications

• Experience working within a clinical trials environment (CRO, pharma or academia)
• Previous experience in Medidata Rave
• Experience in CDISC

Benefits

• Remote working ...