Clincal Data Associate

Specific Responsibilities: Ability to support and/or lead clinical data management activities for several concurrent trials while receiving guidance and direction from Senior Clinical Data Associates or Managers. Identify, track, and resolve data queries while ensuring that study timelines and data quality expectations are met. Ability to utilize, or aptitude for learning to work with electronic data capture and management systems such as Medidata Rave or Phase Forward InForm, and/or to coordinate the outsourcing of CDM services to CROs. Manage clinical data for trials in various stages (set-up, conduct, database freeze/finalization, and archiving), with goal of achieving data quality sufficient for analysis and regulatory submission, by leveraging standard eCRFs and corresponding edit checks, as well as data-review listings. High degree of collaboration required with Clinical and Statistical Programming, Biostatistics, external vendors, and cross-functional study management team members including Clinical Operations, Clinical Research, and Regulatory Affairs.

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