Clinical Research Associate

2 weeks ago


Shanghai, Shanghai, China MakroTech Full time
Role Overview

MakroTech is seeking a highly skilled Clinical Research Associate to manage day-to-day clinical trial activities in Shanghai, China. The ideal candidate will ensure compliance with protocols and regulatory requirements, reviewing clinical trial protocols, and participating in the design and execution of clinical studies.

Key Responsibilities
  • Manage daily clinical trial operations, ensuring compliance with study protocols.
  • Review clinical trial protocols and participate in the design and execution of clinical studies.
  • Collaborate with clinical operations teams, providing support throughout the trial lifecycle.
  • Conduct site monitoring as required, following instructions from the Project Manager.
  • Perform data analysis, interpret results, and contribute to research efforts.
  • Liaise with the medical and scientific community to provide necessary trial support.
Requirements
  • Bachelor's or Master's degree in a related scientific field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • Strong knowledge and hands-on experience in clinical trials and monitoring.
  • Proven ability to create, review, and implement clinical trial protocols.
  • Experience in clinical operations, including site management, monitoring, and data management.
  • Familiarity with Good Clinical Practice (GCP) and International Council for Harmonization (ICH) guidelines.
  • Excellent communication, organizational, and analytical skills.
  • Ability to work independently and remotely.


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