Configuration & QC Specialist I
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring current medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Configuration & QC Specialist I at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to configuration and database systems activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
• Assisting in the configuration and setup of clinical trial databases and electronic data capture (EDC) systems, ensuring accuracy and adherence to project specifications.
• Performing quality control (QC) checks on clinical trial data and study documentation to identify discrepancies, inconsistencies, and data entry errors.
• Collaborating with cross-functional teams including data management, biostatistics, and clinical operations to address QC findings and ensure data integrity and reliability.
• Supporting the development and implementation of validation plans and procedures to assess the functionality and performance of EDC systems and data management processes.
• Providing training and support to end-users on system configuration, data entry guidelines, and QC processes to promote compliance and efficiency.
Your Profile:
You will bring relevant configuration and database systems experience, along with the following qualifications and skills.
Required qualifications and experience:
• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• 1+ years of experience in clinical data management, data entry, or related role, preferably within the pharmaceutical or biotechnology industry.
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