Clinical Research Associate

2 days ago


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

The Clinical Research Associate will be responsible for monitoring and managing research sites to ensure compliance with study protocols, regulations, and sponsor requirements.

Key responsibilities include:

  1. Performing site monitoring visits to verify adherence to protocol and regulatory requirements;
  2. Working with sites to develop and track subject recruitment plans;
  3. Providing training and support to site personnel on protocol and related study procedures;
  4. Evaluating the quality and integrity of site practices and escalating quality issues as necessary;
  5. Managing study progress by tracking regulatory submissions, case report form completion, and data query generation and resolution;
  6. Ensuring accurate documentation of site management, monitoring visit findings, and action plans.
Qualifications

To be successful in this role, you will need:

  1. A Bachelor's Degree in a scientific discipline or healthcare preferred;
  2. At least 1 year of on-site monitoring experience;
  3. Good knowledge of clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines;
  4. Therapeutic and protocol knowledge as provided in company training;
  5. Computer skills, including proficiency in Microsoft Office applications and use of a laptop computer and mobile devices.
About IQVIA Argentina

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate medical treatment development and commercialization, improving patient outcomes and population health worldwide.



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