Clinical research organization seeks Configuration & QC Specialist to design and maintain clinical trial databases and electronic data capture systems. The role involves performing quality control checks on trial data, collaborating with cross-functional teams, and leading validation procedures to ensure regulatory compliance and data integrity.
Responsibilities
Configure and maintain clinical trial databases and EDC systems ensuring accuracy and regulatory compliance
Perform comprehensive quality control checks on clinical trial data and study documentation
Collaborate with data management, biostatistics, and clinical operations teams on QC findings
Lead development and execution of validation plans for EDC systems and data processes




Provide training and guidance to junior team members on configuration and QC best practices
Requirements
Bachelor's degree in scientific or healthcare-related field
3+ years clinical data management, data validation, or pharmaceutical industry experience
Proficiency with EDC systems such as Medidata Rave, Oracle Clinical, or Inform
Strong attention to detail with analytical and problem-solving skills
Excellent communication and interpersonal abilities
Ability to work independently and manage multiple priorities in deadline-driven environment

📌 Configuration & Qc Specialist I And Ii (Xico)
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