Clinical Operations Associate

Job not on LinkedIn

🔥 2 minutes ago

🌐 Brazil, Mexico, +1 more countries – Remote

🇧🇷 Brazil – Remote 🇲🇽 Mexico – Remote 🇨🇴 Colombia – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥 Clinical Operations

👻 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

• Support clinical study teams with administrative and operational tasks • Manage site payments and clinical trial supplies • Maintain and organize essential study documentation within electronic systems • Perform Trial Master File (TMF) related activities to support inspection readiness • Track, collect, scan, file, and process study documents and Case Report Forms (CRFs) • Provide limited site-facing support in partnership with Clinical Research Associates • Work closely with Clinical Research Associates and project teams throughout the clinical trial lifecycle

🎯 Requirements

• Previous experience working at a clinical research site (Site Coordinator, Research Coordinator, or similar roles) • Fluency in English is required • Proficiency with Microsoft Office applications • Ability to manage multiple priorities in a fast-paced environment • Strong organizational skills and attention to detail • A university degree in a healthcare, life sciences, or related field

🏖️ Benefits

• Continuous learning and career development opportunities • Flexible working arrangements • Healthy work-life balance • Collaborative, diverse, and supportive global team • Exposure to a wide range of clinical operations activities and career paths