Description
Join ICON Central Laboratories and play a key role in supporting clinical trials that help bring innovative treatments to patients worldwide. As a Configuration & QC Specialist I, you'll help configure and validate clinical trial laboratory databases, ensuring accuracy, quality, and compliance while partnering with cross-functional teams in a collaborative, fast-paced environment.
Responsibilities
- Support the configuration and setup of clinical trial laboratory databases (LIMS).
- Perform quality control reviews to ensure data accuracy and compliance.
- Investigate and resolve configuration discrepancies.
- Partner with Project Managers, Setup Specialists, and Scientific Affairs teams.
- Maintain accurate documentation and support project deliverables.
- Contribute to continuous improvement initiatives.
Requirements
- Strong attention to detail and analytical skills.
- Excellent communication and organisational abilities.
- Ability to manage multiple priorities in a fast-paced environment.
- Proficiency with Microsoft Office, including Excel.
- Ability to work independently and collaboratively.
Preferred Qualifications
- Experience in configuration, quality control, quality assurance, or data management.
- Experience in healthcare, clinical research, or other regulated environments.
- Familiarity with validation, documentation, and quality processes.
Benefits
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways