Assoc Lab Project Set-up Mgr

IQVIA

Buenos Aires, Argentina
Study database design requirements
Clinical study database configuration
Clinical trial management systems
Manage the design and launch of clinical research studies, owning start-up deliverables and ensuring quality execution across sponsors, CROs, and internal teams

Job Summary

  • Manage the design and launch of clinical research studies, owning start-up deliverables and ensuring quality execution across sponsors, CROs, and internal teams.
  • Develop and manage study database design requirements for protocols, amendments, and sponsor changes, and configure and oversee study databases in alignment with clinical protocols and sponsor standards.
  • We invest in integrated benefits programs and resources to take care of employees’ physical, mental, emotional, financial, and social well-being.

Matching Summary

Manage the design and launch of clinical research studies, owning start-up deliverables and ensuring quality execution across sponsors, CROs, and internal teams.

Skills & Requirements

Must-have

  • study database design requirements
  • clinical study database configuration
  • clinical trial management systems
  • ICH E6 Good Clinical Practice guidelines
  • proactive risk management

Nice-to-have

  • passionate innovators
  • thoughtful and inclusive collaboration
  • accelerate research and development
  • transform healthcare

Key Requirements

  • Bachelor’s degree in science or related field
  • Experience with clinical study database design
  • Working knowledge of CTMS
  • Proficiency with Microsoft Office applications

Work Rights

Not specified

Tailored Resume

Cover Letter