
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.
🕒 May 23
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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.
• Oversee clinical trials, ensuring successful execution from start-up to close-out. • Lead site selection and feasibility assessments, working closely with CRAs and investigators. • Manage study timelines, budgets, and deliverables, ensuring adherence to project objectives. • Provide oversight on protocol administration, site initiation, monitoring, and study progress. • Collaborate cross-functionally with internal and external stakeholders, including sponsors, investigators, and project teams. • Ensure compliance with GCP, FDA regulations, and company SOPs. • Train and mentor CRAs and site staff, ensuring protocol adherence and data integrity.
• Renal experience is mandatory. • Bachelor’s degree in a science-related field (RN preferred) with industry experience, including 1-2 years as a Clinical Trial Manager/Clinical Lead. • Strong background in monitoring and site management, preferably with experience in oncology or other complex indications. • CCRA or CCRP certification is 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 : 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 : Participate in 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 : Be part of a company with international reach, offering you exposure to diverse projects and clients.
Apply Now🕒 April 1
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🕒 April 1
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