Clinical Research Associate II

5 days ago

Guangzhou, Guangdong, China Parexel Full time
Job Description

Overview

Parexel is seeking a highly skilled Clinical Research Associate II to join our team. As a key member of our site management team, you will be responsible for ensuring the successful execution of clinical trials at assigned sites.

Key Responsibilities
  • Start-up Phase: Act as Parexel's direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase.
  • Build Relationships: Build relationships with investigators and site staff.
  • Conduct Site Visits: Conduct, drive, and manage country-specific feasibility and/or site pre-qualification and qualification activities.
  • Generate Reports: Generate visit/contact reports, using judgment to identify site issues and problem-solving to direct resolution.
  • Manage Documents: Develop strategy to configure, distribute, and collect, and review and approve, high-quality country-specific and/or site-specific documents or essential regulatory documents.
  • Ensure Compliance: Monitor and maintain compliance with ICH-GCP and applicable international and local regulations.
Requirements
  • Education: Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience.
  • Experience: Site management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
  • Skills: Sound problem-solving skills, ability to take initiative and work independently, advance presentation skills, client-focused approach to work, and strong computer skills.
What We Offer

Parexel offers a dynamic and challenging work environment, with opportunities for professional growth and development. We are committed to providing our employees with the tools and resources they need to succeed.

Language: English

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