Emerald Clinical
501 - 1000 employees
Founded 2000
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
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.
PMO Analyst
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Emerald Clinical
501 - 1000 employees
Founded 2000
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
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
• Support the implementation and ongoing maintenance of PMO standards, methodologies, and tools across clinical and operational projects • Develop and maintain project dashboards, KPIs, and performance metrics to provide actionable insights • Assist study teams with project timeline tracking and updates • Prepare status reports, presentations, and governance materials for senior leadership and stakeholders • Facilitate project governance processes, including stage gates, audits, and reporting cycles • Collaborate with Project Managers to improve adherence to SOPs, regulatory requirements, and best practices • Analyse project data to identify trends, risks, and opportunities for improvement • Support change management initiatives and continuous improvement efforts across the PMO • Assist in preparing and facilitating Project Management Forum meetings • Contribute to the development and enhancement of tools and processes to support high-quality project documentation • Support project resourcing activities, including coordination for holiday cover
🎯 Requirements
• Bachelor’s degree in Life Sciences, Business Administration, Project Management, or a related field • 2–4 years of experience in a PMO, project coordination, or analytical role, ideally within a CRO or pharmaceutical organisation • Understanding of clinical trial processes and GCP/regulatory frameworks (preferred) • Proficiency in project management tools (e.g., MS Project, Smartsheet) and data analysis tools (e.g., Excel, Power BI) • Strong organisational, analytical, and problem-solving skills • Excellent communication and stakeholder engagement abilities
🏖️ Benefits
• Competitive Compensation: A tailored salary and benefits package reflecting your experience and expertise • Flexibility: Hybrid or remote working options depending on your location • Career Growth: Access to global development opportunities and exposure to leading scientific experts • Employee Wellbeing: Programs designed to support work-life balance, recognition, and team connection • Global Opportunities: Work on international studies with diverse clients and teams
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