Responsibilities:

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.

Requirements:

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.

Katalyst HealthCares and Life Sciences