Clinical Research Associate I

6 days ago


Beijing, Beijing, China Parexel Full time
About the Role

Parexel is seeking a highly skilled Clinical Research Associate I to join our team. As a Clinical Research Associate I, you will be responsible for managing clinical sites, ensuring compliance with regulatory requirements, and executing study protocols.

Key Responsibilities
  • Site Management
    • Build and maintain relationships with investigators and site staff
    • Conduct site qualification and initiation visits
    • Manage site-specific documentation and regulatory submissions
    • Ensure site compliance with study protocols and regulatory requirements
  • Study Execution
    • Develop and implement study plans and strategies
    • Manage site-level data and ensure data quality and integrity
    • Conduct remote visits and contacts as needed
    • Generate visit/contact reports and ensure timely submission
  • Regulatory Compliance
    • Ensure compliance with ICH-GCP and applicable international and local regulations
    • Monitor and maintain regulatory documentation and submissions
    • Collaborate with cross-functional teams to ensure regulatory compliance
Requirements
  • Education
    • Degree in biological science, pharmacy, or other health-related discipline preferred
  • Experience
    • Previous relevant work experience preferred
  • Skills
    • Problem-solving skills
    • Able to work independently and as part of a team
    • Strong communication and interpersonal skills
    • Ability to manage multiple tasks and prioritize
About Parexel

Parexel is a leading global biopharmaceutical services company. We provide a comprehensive range of services to help our clients succeed in the development and delivery of innovative therapies.



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