Configuration & Qc Specialist I And Ii (Xico)

Configuration & Qc Specialist I And Ii (Xico)

17 oct
|
Icon Clinical Research
|
Xico

17 oct

Icon Clinical Research

Xico

Office-Hybrid (3 day at the office) CDMX
ICON is a general healthcare intelligence and clinical research organisation united by a mission to bring new 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 II 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 take responsibility for configuration and database systems deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
Configuring and maintaining clinical trial databases and electronic data capture (EDC) systems, ensuring accuracy, functionality, and compliance with regulatory requirements.
Performing comprehensive quality control (QC) checks on clinical trial data and study documentation, identifying discrepancies, inconsistencies,



and data entry errors.
Collaborating closely with cross-functional teams including data management, biostatistics, and clinical operations to address QC findings and implement corrective actions.
Leading the development and execution of validation plans and procedures to assess the performance and reliability of EDC systems and data management processes.
Providing training, guidance, and support to junior team members on system configuration, data entry guidelines, and QC processes to promote best practices and continuous improvement.
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
3+ years of experience in clinical data management, data validation, or related role, preferably within the pharmaceutic

📌 Configuration & Qc Specialist I And Ii (Xico)
🏢 Icon Clinical Research
📍 Xico

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