Vacancy Description
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 ...
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