Coordonnateur·rice Principal·e De La Mise En Place Des Projets De Laboratoire / Senior Laboratory Project Set-up Coordinator

IQVIA Inc

Mississauga, ON, Canada
Base: $60,000.00 - $100,000.00 annualized; bonus/e...
Not specified (assumed hybrid based on industry norms).
Clinical trial management systems experience
Database configuration and validation skills
Laboratory process knowledge
IQVIA Inc is seeking a Senior Laboratory Project Set-Up Coordinator in Mississauga, ON, to provide operational support for laboratory projects, focusing on clinical study database configuration and compliance. The ideal candidate should possess relevant experience with Clinical Trial Management Systems and strong organizational skills to thrive in a dynamic environment

Job Summary

  • The Senior Laboratory Project Set-Up Coordinator provides project-level laboratory support by configuring, validating, and maintaining clinical study databases while ensuring compliance with procedures and quality standards.
  • Key responsibilities include collaborating with laboratory colleagues to investigate issues, maintaining accurate project documentation, and proactively communicating risks to managers.
  • IQVIA offers integrated benefits programs focused on physical, mental, emotional, financial, and social well-being for employees and their families.

Matching Summary

Match Score: 75

IQVIA Inc is seeking a Senior Laboratory Project Set-Up Coordinator in Mississauga, ON, to provide operational support for laboratory projects, focusing on clinical study database configuration and compliance. The ideal candidate should possess relevant experience with Clinical Trial Management Systems and strong organizational skills to thrive in a dynamic environment.

Salary

Base: $60,000.00 - $100,000.00 annualized; Bonus/Equity: Incentive plans or bonuses may be offered; Benefits: Integrated health, wellness, and social well-being programs

Skills & Requirements

Must-have

  • Clinical Trial Management Systems experience
  • Database configuration and validation skills
  • Laboratory process knowledge
  • Regulatory compliance adherence
  • Project documentation maintenance

Nice-to-have

  • Life Sciences degree preferred
  • Continuous improvement initiative participation
  • Strong written and verbal communication
  • Ability to manage multiple priorities
  • Effective stakeholder relationship building

Key Requirements

  • High School Diploma required
  • Bachelor's degree in Life Sciences preferred
  • Hands-on experience with Clinical Trial Management Systems
  • Knowledge of data management and regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter