Clinical Data Manager Jobs

CDM 340hour engagement | Must be based in Canada

We are seeking a Data Management Specialist who will be responsible for ensuring the accuracy, completeness, and consistency of clinical trial data throughout the study. The ideal candidate will have experience in data management and will be responsible for conducting data reviews, developing data management plans, updating eCRF instructions, and creating user guides. The Data Management Specialist will also work closely with study teams to ensure that data management activities are conducted in compliance with protocol, GCP, and regulatory requirements.

Responsibilities:

• Communicate with study sites to resolve data queries and ensure timely resolution of data issues.
• Conduct monthly data reviews to identify and resolve data discrepancies and data quality issues.
• Reconcile serious adverse events (SAEs) in the database with SAE reports from the clinical site.
• Conduct final data cleaning activities to ensure the accuracy and completeness of study data.
• Develop user guides to assist study personnel in using the study database.
• Update eCRF instruction documents, data management plans, data validation plans, and user guides as needed.
• Develop and maintain eCRF instruction documents, data management plans, and data validation plans.