Senior Cra (sponsor Dedicated)

ICON

Frankfurt, Germany
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and site management
Senior CRA at ICON Plc plays a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards

Job Summary

  • Senior CRA at ICON Plc plays a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • ICON offers a diverse culture that rewards high performance and nurtures talent with competitive salary and a range of benefits focused on well-being and work-life balance.
  • ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.

Matching Summary

Senior CRA at ICON Plc plays a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • Good Clinical Practice (GCP) standards
  • Data integrity and site management
  • Cross-functional team collaboration
  • Travel at least 60% internationally and domestically
  • Valid driver’s license

Nice-to-have

  • Training and guidance to site staff
  • Strong organizational and problem-solving skills
  • Excellent communication and stakeholder management
  • Building effective relationships with site personnel
  • Inclusive and accessible work environment

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive Clinical Research Associate experience
  • Ability to manage multiple sites and projects
  • Proficiency in clinical trial software and tools
  • Ability to travel at least 60%
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter