Clinical Research Associate I/II

Parexel

Clinical Research Associate I/II managing trial conduct and site relationships in Chengdu, China. Ensuring compliance with study protocol and assisting in site management tasks.

Posted 6/26/2026full-timeRemote • 🇨🇳 ChinaJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Act as Parexel’s direct contact with assigned sites
Assess and ensure overall integrity of study implementation and adherence to study protocol
Build relationships with investigators and site staff
Evaluate if on-site staff assignment is still accurate
Apply working knowledge and judgment to identify potential data quality issues
Monitor and maintain compliance with ICH-GCP and applicable regulations
Perform site facilities assessments
Ensure timely and accurate completion of project goals

Requirements

What you’ll need

Site Management experience or equivalent experience in clinical research
Understanding of clinical trials methodology and terminology
Strong problem solving skills
Ability to take initiative and work independently
Experience with Clinical Trial Management System (CTMS)
Strong computer skills including MS-Office products such as Excel and Word
Holds a driver’s license where required

Benefits

Comp & perks

Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

site managementclinical researchclinical trials methodologydata quality assessmentproject goal completion

Soft Skills

problem solvinginitiativeindependencerelationship building

Certifications

driver's license