Clinical Research Associate II

🔥 0 minutes ago

🇵🇱 Poland – 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.

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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

• Conduct qualification, site initiation, monitoring, and termination visits at assigned clinical sites • Generate visit and contact reports • Build and maintain site relationships • Address and resolve site issues and questions as the clinical sites’ sole point of contact • Oversee study integrity and promote rapport with site staff • Review trial performance and safeguard human subjects’ rights and well-being in accordance with protocols • Develop patient recruitment strategies with clinical sites to meet enrollment timelines • Ensure compliance with SOPs, protocols/amendments, GCP, and applicable regulatory requirements • Evaluate reported data quality and integrity, site efficacy, and drug accountability • Monitor completeness and quality of regulatory documentation • Perform site document verification

🎯 Requirements

• Site Management or equivalent experience in clinical research • Understanding of clinical trials methodology and terminology • Ability to perform all clinical monitoring activities independently • Experience with Oncology trials would be an advantage • Bachelor’s or equivalent degree in biological science, pharmacy or another health-related discipline • Strong interpersonal, written, and verbal communication skills within a matrixed team • Self-driven work capacity, sense of urgency, and ability to work with limited oversight • Client-focused approach and flexible attitude toward assignments and new learning • Ability to manage multiple tasks, evaluate unpredictable scenarios, and achieve project timelines • Ability to apply understanding of study protocols • Honest and ethical work approach • Strong computer skills, including CTMS, EDMS, Excel, and Word

🏖️ Benefits

• World class technology and training catered to individual experience • Less travel and a lower protocol load compared to industry peers • Bonus incentive program • Opportunity to work within multiple therapeutic areas • Career advancement opportunities in clinical research • Flexible work