Configuration & Qc Specialist I

ICON Broadbean

Farmingdale, NY, United States
Hybrid
Clinical trial database configuration
Quality control checks
Data integrity and reliability
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 ensuring accuracy and adherence to project specifications.
  • The role involves collaborating with cross-functional teams to address QC findings 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 database configuration
  • quality control checks
  • data integrity and reliability

Nice-to-have

  • strong attention to detail
  • excellent communication skills
  • team-oriented environment

Key Requirements

  • Bachelor's degree in life sciences
  • 1+ years of experience
  • familiarity with LIMS

Work Rights

Not specified

Tailored Resume

Cover Letter