Site Management Specialist

4 days ago


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

This position involves overseeing the conduct of clinical research studies at various sites, ensuring that they are performed in accordance with established protocols, regulations, and sponsor requirements.

Main duties include:

  • Conducting regular site visits to monitor compliance with study protocols and regulatory requirements;
  • Developing and implementing strategies to enhance subject recruitment and retention;
  • Providing guidance and support to site personnel on protocol and related study procedures;
  • Identifying and addressing any quality issues or concerns that may arise during study execution;
  • Collaborating with cross-functional teams to ensure timely completion of study milestones and deliverables.
Required Skills

To succeed in this role, you should possess:

  • A degree in a scientific field or healthcare;
  • Significant experience in on-site monitoring, preferably with at least 1 year of direct involvement;
  • Strong understanding of relevant regulatory frameworks, including GCP and ICH guidelines;
  • Excellent communication and interpersonal skills;
  • Proficiency in MS Office applications and other software tools used in clinical research.
About Our Organization

We are a world leader in providing innovative solutions to the life sciences and healthcare industries. Our mission is to improve human outcomes and patient care through data-driven insights and collaboration.



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