Regulatory Compliance Officer

1 week ago


Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full time

Role Summary

We are seeking an experienced Clinical Research Associate to join our team at IQVIA Argentina. As a key member of our clinical operations team, you will be responsible for ensuring the quality and integrity of clinical trials conducted at our partner sites.

Key Activities

  • Conduct site initiation, monitoring, and close-out visits to assess compliance with study protocols and regulatory requirements.
  • Develop and implement subject recruitment plans to meet project goals.
  • Evaluate site practices related to study conduct and adherence to regulations, escalating issues as necessary.
  • Collaborate with internal teams to support project execution and resolve queries.

Essential Qualifications

  • Bachelor's degree in a scientific discipline or healthcare preferred.
  • At least 1 year of on-site monitoring experience required.
  • Excellent knowledge of GCP and ICH guidelines, as well as therapeutic and protocol knowledge.


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