Clinical Research Associate II

🔥 12 hours ago

🇨🇳 China – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• Conduct source data verification and ensure clinical trial data are submitted to data management promptly • Identify study-conduct issues and ensure appropriate issue closure • Manage investigator site workload and ensure studies run efficiently and meet objectives • Ensure compliance with ICH/GCP, local laws, and client SOPs and procedures • Maintain patient safety and report safety issues according to regulatory requirements • Inform Principal Investigators and site staff of issues • Develop corrective and preventive actions with investigators and site personnel • Manage sites from site selection through study closeout • Train site staff on protocols, amendments, and client processes • Maintain sufficient knowledge of the product, protocol, and therapy area for investigator discussions • Interact with healthcare professionals to enhance client credibility • Ensure monitored data meets quality standards and is entered into client systems promptly • Report study progress after site visits and catalog and manage issues to closure • Maintain accurate site-level information in the clinical trials registry • Obtain and maintain Investigator Initiation Package, Site Master File, ELARA, and/or Trial Master File documentation • Quality-control relevant documents and generate monitoring reports • Maintain monitoring logs • Complete required training, timesheets, expense reports, and CV updates • Comply with Parexel processes, ICH-GCP, and applicable requirements

🎯 Requirements

• Computer Literacy (word processing and spreadsheets, PowerPoint) • Proficient in Chinese • Good command of written and spoken English is required • Good interpersonal skills and communication ability • Flexible attitude with respect to work assignments and new learning; quick learner • Ability to manage multiple and varied tasks, prioritize workload, and maintain attention to detail • Willingness to work in a matrix environment and value teamwork • At least 1.5 years (2 years preferable) of Clinical Monitoring/Site Management experience • Good knowledge of ICH/GCP and relevant international and local regulations relating to Clinical Research • Degree in Life Science, Nursing, Pharmacy, or other relevant education background • Bachelor’s degree or above, or equivalent