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Global Clinical Trial Monitor

1 semana atrás


Lisboa, Lisboa, Portugal Icon Tempo inteiro

We're seeking a highly skilled Clinical Research Associate to join our global team at ICON. This role is perfect for those passionate about advancing healthcare and contributing to cutting-edge clinical trials.

About the Job:

  • You will be responsible for monitoring multiple clinical trial sites, ensuring compliance with regulatory guidelines and best practices.
  • Develop and maintain strong relationships with site staff, fostering a collaborative environment and promoting effective communication.
  • You will provide key project updates and collaborate with the team to develop commitment to study timelines and objectives.
  • Ensure patient safety and data integrity by reviewing source documents and identifying any discrepancies.

What We Offer:

  • A competitive salary and benefits package.
  • The opportunity to work on high-profile clinical trials and contribute to groundbreaking research.
  • A dynamic and inclusive work environment that values diversity and promotes professional growth.