
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.
🔥 1 minute ago
🇺🇸 United States – Remote
💵 $130k - $160k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
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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.
• Oversee clinical trials from start-up to close-out • Lead site selection and feasibility assessments with CRAs and investigators • Manage study timelines, budgets, and deliverables • Provide oversight of protocol administration, site initiation, monitoring, and study progress • Collaborate with sponsors, investigators, internal stakeholders, and project teams • Ensure compliance with GCP, FDA regulations, and company SOPs • Train and mentor CRAs and site staff • Ensure protocol adherence and data integrity
• Renal experience • Bachelor’s degree in a science-related field (RN preferred) with industry experience • 1–2 years as a Clinical Trial Manager/Clinical Lead • Strong background in monitoring and site management • Preferably experience in oncology or other complex indications • CCRA or CCRP certification strongly preferred • Excellent knowledge of GCP, FDA regulations, and clinical trial best practices • Ability to manage multiple projects, timelines, and stakeholders efficiently • Strong leadership, problem-solving, and communication skills • Willingness to travel up to 20% as required
• Competitive compensation with a tailored salary and benefits package • 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 supporting work-life balance, health, and team connection • Global engagement surveys • Recognition programs • Team-building events • Exposure to diverse international projects and clients
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