Clinical Project Manager – Talent Pipeline Opportunity

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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 leadership and oversight for assigned clinical projects from start-up through close-out • Act as the primary point of contact for sponsors, vendors, and internal stakeholders • Develop and maintain study timelines, budgets, forecasts, and project plans • Lead study teams to deliver against quality, budget, and timeline expectations • Identify risks proactively and implement mitigation strategies • Oversee site activation, enrolment performance, monitoring activities, and study execution • Ensure compliance with ICH-GCP, applicable regulatory requirements, and company SOPs • Manage project finances and vendor performance • Support proposal development, business development activities, and bid defense meetings • Mentor and support Clinical Trial Managers, CRAs, and other project team members

🎯 Requirements

• Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or related discipline • Approximately 7+ years of clinical research experience • Minimum 2 years of Project Management experience within a CRO environment • Previous experience managing global or regional studies • Strong client management and stakeholder engagement skills • Proven experience with project budgets and financial oversight • Excellent working knowledge of ICH-GCP and European regulatory requirements • Experience in renal/nephrology clinical trials is highly preferred • Experience across Phase I-IV clinical trials is advantageous

🏖️ 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