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Clinical Research Associate I

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Company NameWuXi PRA Clinical Research (Shanghai) Co., Ltd.
Company TypePrivate
Job TypeFull-Time
Salary RangeMarket Competitive
LocationGuangzhou, Guangdong, China
QualificationsBachelor’s Degree
Experience5 Year+

Job Overview

WuXi PRA Clinical Research (Shanghai) Co., Ltd. is seeking a Clinical Research Associate I to join their dynamic team in Guangzhou, Guangdong, China. This crucial role involves monitoring clinical trials and ensuring the highest standards of research quality within the pharmaceutical manufacturing sector.

Company Overview

WuXi PRA Clinical Research (Shanghai) Co., Ltd. is a joint venture between WuXi AppTec and PRA Health Sciences. It offers comprehensive Phase I-IV clinical trial services across Mainland China, Hong Kong, and the wider Asia region. With strategic offices and staff in 17 cities across China, the company leverages PRA’s extensive global resources, clinical research expertise, global technologies, and standard operating procedures. This centralized operational approach ensures superior quality and outstanding client service, with significant investments in CFDA regulatory expertise, project management, and clinical informatics resources.

Quick Details

  • Salary Range: Market Competitive
  • Job Type: Full-time
  • Qualifications: Bachelor’s Degree
  • Experience: 5 Year+

Key Responsibilities

  • Conduct on-site and remote monitoring visits for clinical trials in compliance with protocols.
  • Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.
  • Verify the accuracy and completeness of clinical data and source documentation.
  • Manage investigational site activities and resolve site-related issues promptly.
  • Provide training and ongoing support to site staff regarding study procedures.
  • Prepare and submit comprehensive monitoring reports and follow-up letters.

Requirements

  • Minimum 5 years of experience in clinical monitoring or a closely related role.
  • Bachelor’s degree in a life science, nursing, or a relevant medical field.
  • Strong knowledge of GCP, ICH guidelines, and CFDA regulatory requirements.
  • Excellent communication, interpersonal, and organizational skills.
  • Ability to work independently and effectively as part of a global team.
  • Proficiency in both English and Mandarin, written and spoken.

Benefits

  • Opportunity to work with a leading global clinical research organization.
  • Exposure to diverse Phase I-IV clinical trials across the Asia region.
  • Significant professional development and career advancement opportunities.
  • Competitive salary and a comprehensive benefits package.
  • A collaborative and supportive international work environment.
  • Contribution to advancements in pharmaceutical manufacturing and patient care.

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