Rave Programmer Analyst - OQSIE

The candidate will function at the level of a Sr. Clinical Programming Analyst using the Medidata Rave EDC system. He/She works with the Clinical Data Manager and other Database clinical programmers in the team to implement and release clinical study databases into production.
Main responsibilities will include, but not limited to,

• Leads development of electronic Case Report Forms (CRFs) based on Clinical Study Design and Specification documentation to support efficient Database Build and Study Migration
• Leads programming of clinical study database edit checks based on Data Validation Specification (DVS) documentation
• Collaborates and assists other database programmers during User Acceptance Testing (UAT) activities
• Reviews and collaborates in defining study specifications, as determined by the Project Teams
• Consults with Clinical Data Manager and other Database Programmers during Clinical Database Start-Up or Database Migration processes on design/specification questions
• May participate in the documentation of clinical database structures, specifications, reports and other database-related tasks during the life of a clinical trial to ensure data quality and compliance with regulatory guidelines and company
• Understands and follows departmental and corporate Work process flows, Standards, Conventions, and SOPs

 

• Must have at least 2+ years of programming experience in Medidata Rave EDC System
• BA Degree is required 
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years') or equivalent combination of education, training, & experience in general clinical data management area.