Clinical Research Associate – Senior, Bilingual French/English

🔥 18 hours ago

🇨🇦 Canada – Remote

⏰ Full Time

🟠 Senior

🧪 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 visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites • Generate visit and contact reports • Build and maintain site relationships as the primary site contact • Address and resolve site issues and questions • Oversee study integrity and site delivery from identification through close-out • Review trial performance and safeguard human-subject rights and well-being in accordance with the protocol • 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

• 18+ months of direct onsite monitoring experience as a Clinical Research Associate (CRA) • 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 • Ability to work independently with a sense of urgency and limited oversight • Client-focused approach and flexibility regarding assignments and new learning • Ability to manage multiple tasks, evaluate unpredictable scenarios, achieve project timelines, and apply understanding of study protocols • Honest and ethical work approach • Strong computer skills, including Clinical Trial Management Systems (CTMS), Electronic Document Management Systems (EDMS), Microsoft Excel, and Microsoft Word • Fluency in written and spoken English and French

🏖️ Benefits

• Bonus incentive program • Less travel and a lower protocol load compared to industry peers • World-class technology • Training catered to individual experience • Opportunity to work within multiple therapeutic areas • Career advancement opportunities • Career growth support through consistent performance discussions and evaluations