Clinical Research Associate

🕒 August 10

🇺🇸 United States – Remote

💵 $110k - $130k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 1%

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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Emerald Clinical

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2000

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Emerald Clinical is a leading global clinical research organization (CRO) founded in the Asia‑Pacific region that provides end‑to‑end clinical trial services to biopharmaceutical, medical device, and diagnostic companies. With about 25 years of experience and a team of 800+ operating across 40+ locations worldwide, Emerald Clinical manages trials across all phases including registration and post‑marketing studies, and offers clinical operations, project management, and trial staffing support. The company emphasizes scientific expertise, operational excellence, and global reach to support drug and device development.

📋 Description

• Conduct qualification, initiation, monitoring, and close-out visits • Ensure patient safety, protocol compliance, and data integrity • Review source data and study documentation • Support site activation and study conduct activities • Build relationships with investigators and site personnel • Contribute to recruitment and retention initiatives • Maintain accurate documentation and reporting according to company requirements • Escalate study risks and issues appropriately

🎯 Requirements

• Bachelor's degree in a scientific or healthcare discipline • Minimum 2 years of on-site monitoring experience • Strong understanding of FDA regulations and ICH-GCP • Proven site management experience • Excellent organizational and communication skills • Ability to travel extensively throughout assigned regions • Experience in renal, nephrology, rare disease, cardiometabolic, or oncology studies preferred

🏖️ Benefits

• Competitive compensation and tailored salary and benefits package • Hybrid or remote working arrangements, depending on location and role • Learning opportunities and access to a global network of scientific leaders • Employee wellbeing programs and initiatives promoting work-life balance, health, and team connection • Global engagement surveys • Recognition programs • Team-building events • Exposure to diverse international projects and clients