Clinical Project Manager- Ivd

IQVIA UK

Base: $93,100.00 - $232,800.00 annualized; bonus/e...
Companion diagnostic (cdx) studies experience
Ivd regulatory knowledge
Eu in vitro device regulation (ivdr)
The Project Lead is responsible for ensuring all studies are designed, planned, executed, monitored, closed out, and documented within the planned timeframe and cost

Job Summary

  • The Project Lead is responsible for ensuring all studies are designed, planned, executed, monitored, closed out, and documented within the planned timeframe and cost.
  • This role involves leading global study teams with full accountability for quality, budget, and timelines while overseeing projects sponsored by Pharma partners.
  • Candidates must ensure adherence to regulations, guidelines, and standard operating procedures while maintaining audit and inspection readiness throughout all study phases.

Matching Summary

The Project Lead is responsible for ensuring all studies are designed, planned, executed, monitored, closed out, and documented within the planned timeframe and cost.

Salary

Base: $93,100.00 - $232,800.00 annualized; Bonus/Equity: Dependent on position offered; Benefits: Range of health and welfare benefits included

Skills & Requirements

Must-have

  • Companion Diagnostic (CDx) studies experience
  • IVD regulatory knowledge
  • EU In Vitro Device Regulation (IVDR)
  • Global study team leadership
  • Budget and timeline management

Nice-to-have

  • Cross-functional collaboration skills
  • Open-minded to new methodologies
  • Strong stakeholder relationship building
  • Experience with CRO oversight

Key Requirements

  • Minimum bachelor's degree in Life Science
  • At least 5 years of relevant industry experience
  • Minimum 1 year project management experience
  • Knowledge of EU IVDR submission process

Work Rights

Not specified

Tailored Resume

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