Clinical Data Science Lead

ICON

Multiple Locations
On-site
Clinical data science initiatives
Manage day-to-day activities
Data collection set-up and review
ICON plc is seeking a Clinical Data Science Lead to manage data science initiatives within clinical trials, ensuring high-quality data analysis for strategic decision-making. The ideal candidate will possess a strong background in clinical data management and project management, with a focus on collaboration and regulatory compliance

Job Summary

  • As a Clinical Data Science Lead at ICON, you will drive data science initiatives within clinical trials, ensuring that our analyses provide meaningful insights that inform strategic decisions.
  • You will manage day-to-day clinical data science activities, supporting your team to deliver quality outcomes.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.

Matching Summary

Match Score: 85

ICON plc is seeking a Clinical Data Science Lead to manage data science initiatives within clinical trials, ensuring high-quality data analysis for strategic decision-making. The ideal candidate will possess a strong background in clinical data management and project management, with a focus on collaboration and regulatory compliance.

Skills & Requirements

Must-have

  • Clinical data science initiatives
  • Manage day-to-day activities
  • Data collection set-up and review
  • Database lock planning and execution
  • Vendor oversight and collaboration
  • Risk mitigation and resolution

Nice-to-have

  • Drive innovation and excellence
  • Foster an inclusive environment
  • Continuous improvement initiatives

Key Requirements

  • Bachelor's degree in life sciences, computer science, or related
  • 4+ years experience in data management/drug development
  • Strong project management skills
  • Knowledge of data management best practices & technologies
  • Understanding of clinical trial documents and processes
  • Knowledge of FDA and ICH regulations
  • Good understanding of CDISC standards
  • Experience with multiple clinical data management systems
  • Good working knowledge of medical coding

Work Rights

Not specified

Tailored Resume

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