Project Manager

🔥 57 minutes ago

🌐 Singapore, Australia, +5 more countries – Remote

🇸🇬 Singapore – Remote 🇦🇺 Australia – Remote 🇨🇳 China – Remote 🇭🇰 Hong Kong – Remote 🇲🇾 Malaysia – Remote 🇹🇼 Taiwan – Remote 🇹🇭 Thailand – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

👷‍♀️ Project Manager

👻 Ghost score 11%

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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

• Develop, conduct and complete clinical research projects according to project originator requirements • Lead and coordinate cross-functional project teams • Manage client communications and relationships • Manage project finances, budgets, forecasts, invoicing and scope changes • Ensure effective resourcing, efficient management, timely delivery and achievement of project objectives • Ensure compliance with Good Clinical Practice, regulatory requirements, SOPs and project-specific documentation • Mentor and coach junior project management staff or Clinical Delivery Leads • Develop project plans and internal project management documents • Support development of protocols and participant information forms • Coordinate feasibility planning and clinical site selection • Identify and support selection of outsourced vendors • Oversee site setup, trial materials, contracts, agreements and site staff readiness • Monitor project progress, milestones, timelines, data quality and data queries • Coordinate study administration, meetings, newsletters, reporting and project documentation • Review and sign off monitoring visit reports • Ensure patient safety and adverse event reporting compliance • Manage study startup, ethics and regulatory submissions, trial management systems and investigator meetings • Coordinate study closeout visits, clinical supply reconciliation and final archiving • Ensure accurate, complete and timely clinical data collection and resolution of data queries • Analyze financial reports and maintain project utilization, revenue forecasts, gross margins and billing timelines • Maintain stakeholder relationships with sponsors, hospitals, professional societies and associations • Contribute to scope change proposals and bid defense presentations • Ensure audit and inspection readiness, quality management compliance, file reviews and co-monitoring requirements

🎯 Requirements

• 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 • 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 and team leadership skills, including leading virtual teams in a cross-cultural environment and dealing with conflict • Strong written and verbal communication skills, including excellent presentation skills

🏖️ Benefits

• Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience • Hybrid or remote working arrangements, depending on your location and role • Access to learning opportunities and 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 projects and clients through international reach

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