
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.
🔥 0 minutes ago
🗣️🇨🇳 Chinese Required
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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.
• Lead contract and budget development across multiple studies • Serve as the main point of contact for sites regarding all contract and budget matters • Oversee site contract negotiations and ensure alignment with sponsor expectations • Partner with clinical operations and project teams to manage timelines, deliverables, and change requests • Coordinate project-specific vendor activities and site payment processes • Track and forecast project budgets, scope changes, and key milestones • Contribute to internal process improvements and support training activities • Ensure compliance with ICH-GCP, SOPs, and all relevant regulatory guidelines
• Qualified lawyer is preferred • Prior experience in a CRO, pharma, or academic setting supporting clinical trials • Strong background in site contract and budget negotiation • Mandarin speaking skills are mandatory for this role. • Excellent interpersonal and communication skills, with experience managing virtual teams • Good understanding of ICH-GCP and clinical research regulations • Proficient in Microsoft Office and clinical trial management tools • Self-motivated, detail-oriented, and adaptable to fast-paced environments.
• 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.
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