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Responsibilities:

  • Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
  • Build and manage strong relationships with trial investigators and stakeholders.

Qualifications:

  • University degree in medicine, science, or equivalent combination of education and experience.
  • Demonstrated ability to drive clinical deliverables of a global study.
  • Experience managing vendor relationships for global clinical studies.

Benefits:

  • Competitive base salary and performance related incentives.
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans, life assurance, and disability coverage.

ICON

ICON is a global healthcare intelligence and clinical research organization that helps bring new medicines and treatments to patients faster. It is a values-driven company with a focus on integrity, collaboration, agility, and inclusion, employing a diverse global workforce.

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