Clinical Research Associate

2 weeks ago


Beijing, Beijing, China Parexel Full time

Job Summary:

Parexel is seeking a skilled Clinical Research Associate to support our clinical trials. As a Clinical Research Associate, you will be responsible for ensuring the integrity and quality of our clinical trials, working closely with site staff, investigators, and other stakeholders.

Key Responsibilities:

  • Conduct site initiation, monitoring, and close-out visits to ensure compliance with study protocols and regulations.
  • Build and maintain relationships with site staff, investigators, and other stakeholders to ensure smooth trial execution.
  • Oversee site-specific documentation, including informed consent forms, clinical site agreements, and other regulatory documents.
  • Manage site-level data, including CRF data entry, query resolution, and SAE reporting.
  • Collaborate with cross-functional teams to ensure timely and effective trial execution.

Requirements:

  • Bachelor's degree in a biological science, pharmacy, or other health-related discipline.
  • Previous experience in clinical research, preferably in a regulatory compliance or site management role.
  • Strong understanding of ICH-GCP guidelines and applicable regulations.
  • Excellent communication, interpersonal, and problem-solving skills.
  • Ability to work independently and as part of a team.

Working at Parexel:

Parexel is a global biopharmaceutical outsourcing services company that provides clinical research, medical communications, and consulting services to pharmaceutical, biotechnology, and medical device companies. Our mission is to improve the lives of patients and healthcare professionals by delivering innovative solutions that accelerate the development and delivery of life-changing therapies.



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