Senior Clinical Trials Coordinator

hace 3 días


Ciudad de México, Ciudad de México Icon Plc A tiempo completo
About Us

At Icon Plc, we're committed to being the world's most comprehensive clinical research organisation. Our success is built on a diverse culture that rewards high performance and nurtures talent.

Job Summary

We're seeking an experienced Clinical Research Associate to join our team As a key member of our clinical operations team, you'll play a vital role in ensuring the integrity of clinical data and the successful conduct of our studies.

Key Responsibilities:
  • Conduct site qualification visits, initiate trials, maintain study files, and provide instructions to site personnel and study close out.
  • Verify the protection of study participants by confirming informed consent procedures and protocol adherence.
  • Ensure clinical data integrity and compliance with approved protocols, GCP, applicable regulations, and SOPs.
  • Manage Investigational Product (IP) properly and write and submit reports of investigational site findings.
  • Escalate observed deficiencies, issues, and corrective action plans as appropriate.
Requirements:
  • 1+ years of experience supporting clinical trials, including onsite monitoring experience.
  • In-depth knowledge of the drug development process and ICH-GCP guidelines.
  • Sound knowledge of applicable policies, procedures, SOPs, and work instructions.
  • Excellent communication, interpersonal, and time management skills.
  • Ability to focus on detail for extended periods and travel extensively.
What We Offer:

Competitive salary: $65,000 - $85,000 per year, depending on location and experience.

A range of health insurance options to suit your needs.

Annual leave entitlements, retirement planning, and employee assistance programs.

A chance to work with a global leader in clinical research and development.



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