Clinical Data Management & Technology Contractor

Cambridge, MA | Contract

Post Date: 06/27/2018 Job ID: 226704 Industry: IT

This role manages all aspects of the clinical trial data management process from study start up to database lock for trials conducted through an outsourced partner / Contract Resource Organization (CRO) 

Duties and Responsibilities: 
• Acts as the data expert and represents CDMT on study team as applicable 
• Works with CRO to ensure data collection tools capture protocol requirements 
• Identifies and resolves data flow process issues in collaboration with the project team 
• Defines data handling conventions, quality acceptance and auditing criteria for data collection and data deliverables 
• Provides guidance and sponsor approval per CRO SOPs and process exceptions 
• Serves as an internal CDMT expert for cross functional team members 
• Liaises with third-party vendors in support of study team escalations 
• Monitors timelines to ensure data management-related deadlines or contributions to study deliverables are proactively defined and met 

• Must have 10-15 years of experience 


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