Clinical Research Associate II – CART

Parexel

Clinical Research Associate II driving study performance and monitoring site compliance at Parexel. Collaborating with investigators and local teams to ensure data quality and adherence to regulatory standards.

Posted 5/30/2026full-timeRemote • 🇨🇳 ChinaJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Drive study performance at the sites.
Perform site monitoring and other onsite visit activities according to monitoring plan and in compliance with procedural documents.
Provide the required monitoring visit reports within required timelines.
Proactively identify study-related issues and escalates to Local Study Teams as appropriate.
Contribute to the selection of potential sites and investigators.
Train, support and advise Investigators and site staff in study related matters.
Obtain and maintain essential documentation in compliance with ICH-GCP, Procedural Documents and local regulations.
Manage study supplies, drug supplies and drug accountability at study sites.
Perform source data verification according to SDV plan.
Ensure data query resolution.
Work with data management to ensure quality of the study data.
Ensure accurate and timely reporting of Serious Adverse Events.
Share relevant information on patient recruitment and study site progress within local Study Team.
Update VCV and other systems with data from centers as per required timelines.
Prepare for activities associated with audits and regulatory inspections in liaison with local Study Team Lead and QA.

Requirements

What you’ll need

Minimum 2-year experience as CRA, performed all tasks for a CRA position
Read, write, and speak fluent English; fluent in host country language required.
Bachelor's degree in biological science or healthcare-related field., or equivalent

Benefits

Comp & perks

Health insurance
Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

site monitoringsource data verificationdata query resolutionstudy performance managementdrug accountabilitymonitoring visit reportingstudy supplies managementessential documentation maintenanceICH-GCP complianceregulatory inspection preparation

Soft Skills

problem identificationcommunicationtrainingsupportadvisingteam collaborationproactive issue escalationorganizational skillstimelinessattention to detail