Configuration & QC Specialist I

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a Configuration & QC Specialist I at ICON Central Laboratories (ICL), you will play a pivotal role in building and amending laboratory specifications within the clinical trial database (LIMs), contributing to the advancement of innovative treatments and therapies.

Responsibilities

• Assist ICL Project Managers and Setup Specialists in the configuration and setup of clinical trial laboratory database ensuring accuracy and adherence to project specifications.
• Perform quality control (QC) checks on clinical trial database and study documentation to identify discrepancies, inconsistencies, and data entry errors.
• Collaborate with cross-functional teams including ICL Project Management, ICL Setup Specialists and Scientific Affairs to address QC findings and ensure data integrity and reliability.

Requirements

• Bachelor's degree in life sciences or related field
• 1+ years of experience in clinical data management, data entry, a laboratory environment or related role, preferably within the pharmaceutical or biotechnology industry.
• Familiarity with information management systems (such as LIMS).
• Strong attention to detail and analytical skills, with the ability to identify and resolve data-related issues.
• Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.
• Proactive attitude with a willingness to learn and adapt to evolving technologies and processes.

Rewards & 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