Clinical Research Associate II – FSP

🔥 0 minutes ago

🇨🇳 China – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

👻 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

• Implement and monitor clinical trials to ensure sponsor and investigator obligations are met and comply with local regulatory requirements and ICH GCP guidelines • Assess potential investigative site qualifications and initiate, instruct, monitor, and close clinical trials at investigative sites • Review and verify the accuracy of clinical trial data collected onsite or remotely • Provide regular site status information to team members and trial management, and update trial management tools • Complete monitoring activity documents according to SOPs and contractual obligations • Collaborate with clinical team members to resolve trial and clinical issues promptly • Escalate site and trial issues according to SOPs until resolved or closed • Reconcile essential document site files • Perform source document verification and query resolution • Assess investigational product accountability, dispensation, and compliance • Verify SAE reporting according to trial specifications and ICH GCP guidelines • Communicate with investigative sites and update tracking systems • Ensure required training is completed and documented • Serve as the main observer/assessor of site activities • Facilitate audits and audit resolution • Perform related duties such as protocol amendment submissions and investigator site budget negotiation • Mentor junior-level CRAs and serve as a resource for new employees • Support site performance responsibilities and additional clinical operations tasks • Interact with other functional areas to resolve site issues and facilitate trial timelines • Perform clinical tasks requiring advanced negotiating skills

🎯 Requirements