Director Of Ivd Clinical Affairs

IQVIA UK

Base: $122,000.00 - $339,700.00 annualized; bonus/...
Not specified
7-10 years clinical research experience
5 years direct ivd clinical trial experience
4 years people leadership experience
IQVIA UK is seeking a Director of IVD Clinical Affairs to lead and oversee In-Vitro Diagnostics clinical trials. This senior role involves strategic leadership, operational oversight, and collaboration with sponsors to ensure compliance and successful execution of IVD studies

Job Summary

  • This senior clinical leadership role provides scientific, regulatory, and operational oversight of In-Vitro Diagnostics (IVD) clinical trials.
  • The position requires deep working knowledge of IVD clinical trial design, execution, and evolving regulatory expectations while ensuring GCP compliance.
  • Candidates will drive IQVIA's IVD CRO capabilities by managing sponsor relationships, leading teams, and supporting business development initiatives.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Director of IVD Clinical Affairs to lead and oversee In-Vitro Diagnostics clinical trials. This senior role involves strategic leadership, operational oversight, and collaboration with sponsors to ensure compliance and successful execution of IVD studies.

Salary

Base: $122,000.00 - $339,700.00 annualized; Bonus/Equity: Dependent on position offered; Benefits: Range of health and welfare benefits available

Skills & Requirements

Must-have

  • 7-10 years clinical research experience
  • 5 years direct IVD clinical trial experience
  • 4 years people leadership experience
  • GCP and IVD regulatory expertise
  • Sponsor relationship management

Nice-to-have

  • Experience with EDC and CTMS systems
  • Strong strategic business development skills
  • Ability to lead high-complexity studies
  • Cross-functional alignment capabilities

Key Requirements

  • Bachelor's degree in healthcare or life sciences
  • Minimum 7-10 years clinical research experience
  • At least 5 years direct IVD clinical trial experience
  • Minimum 4 years supervisory leadership experience
  • Expert-level understanding of GCP and CRO operations

Work Rights

Not specified

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