Clinical Research Associate

2 months ago


Singapur, Singapore IQVIA Full time
Job Summary

We are seeking a highly skilled Clinical Research Associate to join our team at IQVIA. As a Clinical Research Associate, you will be responsible for managing the progress of assigned studies, tracking regulatory submissions and approvals, and ensuring the quality and integrity of study site practices.

Key Responsibilities
  • Perform site selection, initiation, monitoring, and close-out visits in accordance with contracted scope of work and good clinical practice.
  • Provide monitoring visits and site management for a variety of protocols, sites, and therapeutic areas.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans.
Requirements
  • Bachelor's degree in a health care or other scientific discipline or educational equivalent.
  • Minimum of 1+ years of on-site monitoring experience; or equivalent combination of education, training, and experience.
  • Computer skills including proficiency in use of Microsoft Word, Excel, and PowerPoint and use of a laptop computer.
  • Good written and verbal communication skills.
  • Good organizational and problem-solving skills.
  • Effective time management skills.

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.



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