Clinical Trial Assistant – FSP

🔥 0 minutes ago

🇨🇳 China – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Clinical Trial Assistant

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Assist with site activation, including vendor-system access, quarterly access reconciliation, staff training follow-up, Investigator’s Site File printing and shipment, and material/equipment shipments • Provide requested project data to the clinical project leadership team • Maintain the Trial Master File, upload documents on time, update the Expected Document List, and address Quality Issues • Follow up with site and internal study team members on pending documents, information, trainings, EDC data, safety-information verification, and actions • Transfer documents to sponsor TMF systems when applicable • Support investigator payment management • Address site issues to closure and assist CRAs with site-management issue resolution • Update CTMS, study systems, and trackers with site information for trial progress tracking • Identify potential issues, provide feedback to study teams, and follow study timelines • Coordinate equipment returns and assist with database lock and administrative site closeout activities • Maintain compliance with ICH-GCP, local regulations, Parexel procedures, and study-specific requirements • Complete administrative tasks such as timesheets, trainings, assessments, and metrics • Participate as a process or platform Subject Matter Expert with minimal line-manager oversight • Mentor and train less experienced staff as appropriate

🎯 Requirements

• Strong command of written and spoken English language; local language proficiency as required • Strong computer and internet skills, including CTMS, EDMS, MS Office products such as Excel, Word, PowerPoint, Outlook, and WebEx • Good organizational skills and meticulous attention to detail • Ability to manage multiple tasks and prioritize work to achieve project timelines • Effective problem-solving skills • Good oral and written communication skills • Basic knowledge and compliance with applicable ICH-GCP Guidelines, international and local regulations, and Parexel procedures • Ability to work independently, seek guidance when necessary, and escalate issues as required • Relevant qualification or equivalent experience required • Previous clinical research experience preferred • High school diploma or higher, ideally a degree in life science or another related background, preferred