As a C&Q Specialist I at ICON Central Laboratories, you will play a pivotal role in building and amending laboratory specifications within the clinical trial database
Job Summary
As a C&Q Specialist I at ICON Central Laboratories, you will play a pivotal role in building and amending laboratory specifications within the clinical trial database.
You will assist project managers and setup specialists in configuration and setup of clinical trial laboratory databases ensuring accuracy and adherence to project specifications.
The role involves performing quality control checks on clinical trial databases and study documentation to identify discrepancies and ensure data integrity.
Matching Summary
As a C&Q Specialist I at ICON Central Laboratories, you will play a pivotal role in building and amending laboratory specifications within the clinical trial database.
Skills & Requirements
Must-have
clinical trial laboratory database setup
quality control checks on clinical data
familiarity with LIMS
data integrity and reliability
collaboration with cross-functional teams
Nice-to-have
strong attention to detail
analytical skills
excellent communication skills
proactive attitude
team-oriented environment
Key Requirements
Bachelor's degree in life sciences or related field
1+ years experience in clinical data management or related role
experience in pharmaceutical or biotechnology industry preferred