Senior Laboratory Project Set-up Coordinator

IQVIA Inc

Marietta, GA, US
Base: $51,800.00 - $108,000.00; bonus/equity: depe...
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Hands-on experience with clinical trial management systems
Understanding of laboratory processes and study set-up workflows
Proficiency in standard computer applications including spreadsheets
** IQVIA Inc. is seeking a Senior Laboratory Project Set-Up Coordinator for its Marietta, GA location. The role involves configuring and validating laboratory databases within Clinical Trial Management Systems, ensuring compliance and quality standards while collaborating with cross-functional teams. **

Job Summary

  • The Senior Laboratory Project Set-Up Coordinator provides project-related support by configuring, validating, and maintaining laboratory databases within Clinical Trial Management Systems.
  • IQVIA is a leading global provider of clinical research services committed to transforming and accelerating research and development through thoughtful collaboration.
  • The role offers a potential base pay range of $51,800.00 to $108,000.00 along with integrated benefits programs for physical, mental, and financial well-being.

Matching Summary

Match Score: 75

** IQVIA Inc. is seeking a Senior Laboratory Project Set-Up Coordinator for its Marietta, GA location. The role involves configuring and validating laboratory databases within Clinical Trial Management Systems, ensuring compliance and quality standards while collaborating with cross-functional teams. **

Salary

Base: $51,800.00 - $108,000.00; Bonus/Equity: Dependent on position offered; Benefits: Integrated benefits programs included

Skills & Requirements

Must-have

  • Hands-on experience with Clinical Trial Management Systems
  • Understanding of laboratory processes and study set-up workflows
  • Proficiency in standard computer applications including spreadsheets

Nice-to-have

  • Bachelor's degree in Life Sciences or related field
  • Strong organizational and coordination skills
  • Ability to work effectively in a fast-paced environment

Key Requirements

  • High School Diploma or equivalent required
  • Experience with Clinical Trial Management Systems
  • Understanding of validation activities

Work Rights

Not specified

Tailored Resume

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