Configuration & QC Specialist I – Clinical Data Management
Job Requisition ID: JR140312
Employment Type: Full Time
Work Mode: Office-Based with Flexible Work Options
Location: Bengaluru, India
Experience Required: 1–3 Years
Job Overview
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Configuration & QC Specialist I to support clinical trial data systems and quality assurance activities. This role plays a critical part in ensuring the accuracy, integrity, and compliance of clinical trial databases and electronic data capture (EDC) systems across global research programs.
The position is ideal for professionals looking to build a strong foundation in clinical data management, system configuration, and quality control within a regulated clinical research environment.
Key Responsibilities
Clinical Database Configuration & Support
Assist in the configuration, setup, and maintenance of clinical trial databases and EDC systems in alignment with approved study specifications and protocols.
Support system build activities to ensure accuracy, consistency, and compliance with data management standards.
Quality Control & Data Integrity
Perform quality control (QC) checks on clinical trial data and study documentation to identify discrepancies, inconsistencies, and data entry errors.
Document and track QC findings, supporting timely resolution in collaboration with cross-functional teams.
Cross-Functional Collaboration
Work closely with data management, biostatistics, and clinical operations teams to address QC issues and ensure reliable, high-quality data deliverables.
Support validation activities to assess system functionality, performance, and compliance.
Training & Process Support
Provide guidance and support to end users on system configuration, data entry standards, and QC procedures.
Contribute to the continuous improvement of data management and validation processes.
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Computer Science, Clinical Research, or a related discipline.
Minimum 1–3 years of relevant experience in clinical data management, data entry, database configuration, or a related role within a pharmaceutical, biotechnology, or CRO environment.
Hands-on exposure to EDC platforms such as Medidata Rave, Oracle Clinical, or Inform is highly desirable.
Skills & Competencies
Strong attention to detail with excellent analytical and problem-solving skills.
Ability to identify, analyze, and resolve data-related issues efficiently.
Effective written and verbal communication skills with the ability to work collaboratively in team-oriented environments.
Proactive mindset with a willingness to learn and adapt to evolving clinical technologies and processes.
Why Join ICON
ICON offers a supportive and inclusive workplace that values innovation, quality, and professional development. Employees benefit from competitive compensation, flexible work arrangements, and comprehensive benefits designed to support personal well-being and long-term career growth.
ICON is an equal opportunity employer committed to fostering diversity, equity, and inclusion across its global workforce.
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