
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.
🔥 48 minutes ago
🌐 Singapore, Australia, +5 more countries – Remote
⏰ Full Time
🟠 Senior
🔴 Lead
👷♀️ Project Manager
👻 Ghost score 11%
Where this job comes from
Posted on Emerald Clinical's careers page, not through a job board
First seen by Remote Rocketship 48 minutes ago
Still open on Emerald Clinical's site. Checked 36 minutes ago.

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.
• Develop, conduct, manage, and complete clinical research projects according to project requirements • Lead and coordinate cross-functional project teams and manage client communications • Manage project budgets, scope, timelines, resources, milestones, reporting, and invoicing • Coordinate feasibility planning, site selection, site setup, monitoring, and site management • Develop project plans, study management documents, site manuals, operating procedures, monitoring plans, and trial management systems • Coordinate study startup, investigator meetings, ethics and regulatory submissions, and study closeout • Ensure site staff receive required materials and training, including data management tools and principles • Drive accurate, complete, clean, and verifiable data collection and resolve data queries • Ensure patient safety and appropriate reporting of adverse and serious adverse events • Manage clinical data, essential documents, study materials, filing, archiving, and document reconciliation • Analyze project financial reports, forecasts, utilization, revenue recognition, margins, billing, and scope changes • Maintain relationships with sponsors, investigators, vendors, hospitals, professional societies, internal teams, and academic leads • Contribute to proposals and bid defense presentations and support business development • Ensure compliance with ICH-GCP, SOPs, regulatory requirements, quality management strategy, audits, inspections, and file reviews • Mentor and coach junior project management staff or Clinical Delivery Leads
• Bachelor’s or Masters degree in a science or related field • Previous experience working on clinical projects within an academic, CRO or pharmaceutical company environment • Approximately seven (7) years of industry experience recommended for this role • 1–2 years of Project Management experience • Prior CRA experience preferred, or site management role experience, trial coordination or relevant industry experience required • Experience managing early-phase and healthy volunteer studies is a plus, not mandatory • Experience managing single or different regions and working across different therapeutic indications • Experience managing full-service studies • Excellent working knowledge of, and ability to implement project activities in accordance with, ICH/GCP and all applicable regulations and guidelines in the relevant regions • Previous exposure to client-facing interactions and/or client management • Project finance management experience • Excellent interpersonal, presentation, communication, and team leadership skills, including leading virtual teams in a cross-cultural environment and dealing with conflict
• Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience • Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role • Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role • Employee Wellbeing: Programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events • Global Opportunities: Exposure to diverse projects and clients through the company's international reach • Purpose-driven work contributing to clinical trials that improve lives • Collaboration and innovation culture valuing diverse perspectives and creative solutions
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