Clinical Research Associate

hace 4 días


Colombia ICON A tiempo completo

At ICON, we're a global leader in clinical research, and as a Clinical Research Associate - Regulatory Compliance Specialist, you'll play a vital role in ensuring the integrity of our studies.

We're looking for an experienced professional to join our team and support our oncology projects. The ideal candidate will have at least 2 years of on-site monitoring experience and a Bachelor's degree in a health, life sciences, or relevant field.

As a Clinical Research Associate, your primary responsibility will be to ensure that all study procedures are conducted in accordance with approved protocols, GCP, and applicable regulations. You'll also be responsible for verifying the protection of study participants and ensuring the integrity of clinical data.

In this role, you'll work closely with cross-functional teams to identify and address any deviations from protocol or regulatory requirements. Your attention to detail and ability to communicate effectively will be essential in maintaining high-quality standards.

What can you expect from this role?

  • Completes onsite and remote monitoring activities according to ICH-GCP guidelines and applicable regulations
  • Verifies informed consent procedures and protocol adherence
  • Ensures study integrity and compliance with approved protocol, GCP, and SOPs
  • Writes and submits reports of investigational site findings and updates tracking systems
  • Escalates observed deficiencies and issues

You'll also have opportunities to develop your skills and contribute to the success of our organization.

What we offer:

  • An estimated salary range of $80,000-$110,000 per year, based on location and experience
  • A competitive benefits package, including medical, dental, and vision insurance
  • A 401(k) plan with company match
  • Generous paid time off and holidays

If you're passionate about clinical research and want to join a dynamic team, apply today



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