Senior Clinical Research Associate - FSP

Posted 17ds ago

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Job Description

Overseeing monitoring responsibilities and ensuring proper conduct of clinical trials at Parexel. Collaborating with sites and managing operational aspects of clinical research in South Korea.

Responsibilities:

  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock
  • Serve as the primary point of contact for assigned investigator sites
  • Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators

Requirements:

  • Minimum 3 years relevant experience in clinical research site monitoring
  • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
  • Fluent in English and in the native language(s) of the country they will work in
  • Bachelor's degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent

Benefits:

  • Health insurance
  • Professional development opportunities
  • Significant travel is required