Senior Medical Monitor Manager

🔥 3 minutes ago

🇸🇬 Singapore – Remote

⏰ Full Time

🟠 Senior

👔 Manager

👻 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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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 in accordance with GCP and study protocols • Act as senior medical contact for clinical development, protocol input, medical review, safety assessment, and client/regulatory interactions • Review and provide medical input on protocols, informed consent forms, Investigator’s Brochures, statistical analysis plans, and other study documents • Participate in study start-up, monitoring, and closeout activities as needed • Provide medical training and support to monitors and project teams, including investigator meetings and safety/data monitoring committees • Conduct medical review of clinical data and identify data quality or safety issues • Assess and manage adverse events and serious adverse events, including medical adjudication, causality assessment, and follow-up recommendations • Prepare and review medical reports • Communicate with investigators, sponsors, safety monitoring committees, pharmacovigilance teams, and regulatory authorities • Serve as company medical representative in client meetings, RFPs, and communications with ethics committees and regulators • Conduct product safety monitoring and prepare or review safety reports, Risk Management Plans, DSURs, and PSURs • Collaborate with Medical Directors/Managers and drug safety teams to evaluate and resolve safety issues • Complete other activities assigned by the Medical Director

🎯 Requirements

• Master degree in Medicine • Minimum 2 years of hands-on medical practice experience, excluding experience gained during postgraduate studies • 7–10 years or above working experience • 5+ years of medical monitoring or medical manager experience • CRO or sponsor experience preferred • Fluent verbal and written English • Ability to work independently and handle multiple tasks simultaneously under pressure • Excellent communication, cross-functional coordination, and problem-solving skills • Global, cross-cultural perspective and customer-oriented approach • Knowledge of GCP and clinical trial processes • Ability to communicate with international clients and regulators

🏖️ 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 • 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