Clinical Research Associate II, Senior Clinical Research Associate

🕒 October 18, 2025

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 55%

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 visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites • Generate visit and contact reports • Build and maintain site relationships and serve as the site's primary point of contact • Address and resolve site issues and questions • Manage site quality and delivery from site identification through close-out • Oversee study integrity and promote rapport with clinical sites and staff • Review trial performance and safeguard the rights and well-being of human subjects • Develop patient recruitment strategies with clinical sites to meet enrollment timelines • Ensure compliance with SOPs, protocols and 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, with understanding of clinical trials methodology and terminology • Ability to perform all clinical monitoring activities independently • Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline • Strong interpersonal, written, and verbal communication skills within a matrixed team • Experience working in a self-driven capacity, with a sense of urgency and limited oversight • Client-focused approach to work and flexible attitude with respect to assignments/new learning • Ability to manage multiple tasks, evaluate unpredictable scenarios, and achieve project timelines while applying understanding of study protocols • Honest and ethical work approach • Strong computer skills, including Clinical Trial Management Systems (CTMS), Electronic Document Management Systems (EDMS), and Microsoft Excel and Word • Ability to work in the UK

🏖️ Benefits

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