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CRA1

ICON · Shanghai, China

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Clinical OperationsFull-timeCompany career page

The apply link worked recently (not employer-confirmed).

Role summary

A Clinical Research Associate is needed in Shanghai to oversee trial coordination, monitor study activities, and ensure regulatory compliance. The role involves managing site relationships, processing sponsor queries, and maintaining documentation while traveling 60% of the time. Candidates require a science degree, ICH-GCP knowledge, strong English communication, and valid driving license.

What they're looking for

  • University degree in medicine, science, or equivalent field
  • Knowledge of ICH-GCP guidelines and medical data review expertise
  • Excellent written and verbal English communication skills
  • Strong interpersonal skills for timely stakeholder query management
  • Ability to travel 60% of time internationally and domestically
  • Valid driver's license required

What you'll be doing

  • Coordinate clinical trial setup and monitoring activities independently
  • Complete accurate study status reports and maintain study documentation
  • Process sponsor-generated queries and manage study cost efficiency
  • Prepare and review study documentation and feasibility assessments
  • Ensure patient safety and regulatory compliance with protocols and procedures

Privacy & handoff

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RoleLantern checkedNeeds clarity
Date posted30 days ago
Last source checkToday
Salary listedNeeds clarity
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