Description
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