Senior Cra

ICON

Singapore, Singapore
On-site
Clinical trial site monitoring
Adherence to study protocols
Gcp standards compliance
ICON plc is seeking a Senior Clinical Research Associate (CRA) in Singapore to oversee clinical trial activities, ensuring compliance with regulatory requirements and industry standards. The role requires extensive CRA experience and offers a range of competitive benefits in an inclusive work environment

Job Summary

  • As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
  • In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance.

Matching Summary

Match Score: 85

ICON plc is seeking a Senior Clinical Research Associate (CRA) in Singapore to oversee clinical trial activities, ensuring compliance with regulatory requirements and industry standards. The role requires extensive CRA experience and offers a range of competitive benefits in an inclusive work environment.

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • Adherence to study protocols
  • GCP standards compliance
  • Data integrity assurance
  • Participant safety oversight

Nice-to-have

  • Cross-functional team collaboration
  • Effective stakeholder management
  • Fostering inclusive environment
  • Driving innovation and excellence

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites and projects
  • Ability to travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

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