Job Description

• Develop and review data management procedures for clinical trials with sponsor companies and other departments.
• Design reports and metrics that are useful management tools for your projects.
• Lead the design and validation of the CRF specifications and edit checks for the electronic data capture system used for each study.
• Attend and participate in teleconferences and face-to-face meetings with sponsor companies as the lead representative from data management.
• Creates and oversees EDC build and database lock timelines in order to maintain on-time deliverables.
• May provide project data management training as needed regarding CRF Completion or EDC system usage.
• Manage multiple projects and associated project team members.
• Coordinate overall data management by serving as primary contact for the sponsor, external data providers, and all project team members.

• At least seven (7) years of Data Management experience.
• At least two (2) years of direct client support and contact.
• At least two (2) years of CRO experience.
• Computer experience with database, spreadsheet, and analysis software (i.e, Rave or SAS preferred).
• Possess an understanding of database structure and processes in data management.
• A basic knowledge of medical terminology is needed, as well as knowledge of clinical research methodologies.

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