Associate Lab Project Set-up Manager

IQVIA

Collegeville, United States
Base: $62,000.00 - $129,100.00; bonus/equity: ince...
Fully remote
Clinical study database configuration
Study start-up processes
Clinical trial management systems
The Clinical Study Start-Up Manager leads the design, configuration, and launch of clinical research studies, ensuring high-quality sponsor deliverables while coordinating cross‑functional teams and supporting business growth initiatives

Job Summary

  • The Clinical Study Start-Up Manager leads the design, configuration, and launch of clinical research studies, ensuring high-quality sponsor deliverables while coordinating cross‑functional teams and supporting business growth initiatives.
  • We invest in integrated benefits programs and resources to take care of our employees’ physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

The Clinical Study Start-Up Manager leads the design, configuration, and launch of clinical research studies, ensuring high-quality sponsor deliverables while coordinating cross‑functional teams and supporting business growth initiatives.

Salary

Base: $62,000.00 - $129,100.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Health and welfare and/or other benefits

Skills & Requirements

Must-have

  • clinical study database configuration
  • study start-up processes
  • Clinical Trial Management Systems
  • manage multiple priorities
  • medical and clinical research terminology

Nice-to-have

  • passionate innovators
  • thoughtful and inclusive collaboration
  • accelerate research and development
  • proactively identify scope changes

Key Requirements

  • Bachelor’s degree in science or related field
  • Hands-on experience with clinical study database configuration
  • Demonstrated experience managing Phase I–IV clinical trials
  • Proficiency with Microsoft Office applications

Work Rights

Not specified

Tailored Resume

Cover Letter