Medical Monitor

🔥 4 minutes ago

🇰🇷 South Korea – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 11%

What it means: the chance that no one is really hiring for this job.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

• Provide medical oversight and support for clinical trials, ensuring studies are conducted safely, compliantly and scientifically according to GCP and protocol • Serve as the medical/clinical expert for study design, conduct, data interpretation and safety evaluation • Provide medical and academic expertise for new and existing studies • Support Endpoint Adjudication and other relevant committees • Provide medical input to safety, endpoint documents and project plans • Represent Emerald Clinical with academic colleagues, customers, vendors, government and regulatory bodies • Ensure activities comply with relevant Acts, legal requirements and ethical standards • Contribute clinical input to protocols, procedure manuals, data collection tools and data quality plans • Review database query reports to identify errors and inconsistencies • Provide ongoing medical support to sites regarding patient eligibility, recruitment, treatment, management and adverse events • Develop and provide protocol training for investigators and CRAs • Contribute to investigator training and education materials • Liaise with project teams, data management, endpoint coordinators, investigators, site staff, sponsors and endpoint adjudicators • Contribute to endpoint adjudication manuals, plans, charters, tracking tools and documentation • Provide medical review and input to endpoint packages • Contribute to safety manuals, plans, charters, tracking tools and documentation • Review and provide narratives for Serious Adverse Events where contracted • Provide medical advice and guidance to the Safety team • Contribute to therapeutic-area training for Emerald Clinical staff • Review literature and participate in research related to Emerald Clinical’s activities or interests

🎯 Requirements

• Tertiary qualifications in Medicine, Pharmacy or life sciences education background • Master’s degree or above preferred • Minimum of 3+ years of experience in medical monitoring or medical management • Fluent verbal and written English • Mandarin speaking skill highly regarded • Working knowledge of current ICH/GCP, ethical and regulatory requirements • Excellent attention to detail and accuracy • Highly developed interpersonal, relationship-building and negotiation skills • Ability to work independently and in a team environment • Ability to perform multiple tasks and prioritize work effectively

🏖️ Benefits

• Competitive salary and benefits package tailored to skills and experience • Hybrid or remote working arrangements, depending on location and role • Learning opportunities and access to a global network of scientific leaders • Global engagement surveys • Recognition programs • Team-building events • Exposure to diverse projects and clients through international reach

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