
501 - 1000 employees
Founded 2000
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą Logistics
Emerald Clinical is a leading global clinical research organization (CRO) founded in the AsiaâPacific region that provides endâtoâend 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 postâmarketing 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.
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501 - 1000 employees
Founded 2000
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą Logistics
Emerald Clinical is a leading global clinical research organization (CRO) founded in the AsiaâPacific region that provides endâtoâend 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 postâmarketing 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.
âą Conduct site qualification, initiation, routine monitoring, and close-out visits âą Ensure protocol compliance and patient safety âą Review source documentation and validate study data âą Support investigator sites throughout the clinical trial lifecycle âą Manage site relationships and provide training as required âą Ensure timely issue identification and escalation âą Maintain high-quality documentation within study systems and TMF âą Support recruitment and retention initiatives âą Join a talent pipeline for future projects and resource requirements as study awards and business needs emerge
âą Degree qualification in Life Sciences or a healthcare-related discipline âą Minimum 2 years of independent monitoring experience âą Experience within CRO, academic research, or pharmaceutical environments âą Strong knowledge of ICH-GCP and European regulatory requirements âą Excellent communication and relationship-building skills âą Ability to travel regionally âą Experience in renal, nephrology, cardiometabolic, or oncology studies preferred
âą Competitive salary and benefits package tailored to skills and experience âą Hybrid or remote working arrangements, depending on location and role âą Learning opportunities and access to a global network of scientific leaders âą Employee wellbeing programs and initiatives promoting work-life balance, health, and team connection âą Global engagement surveys âą Recognition programs âą Team-building events âą Exposure to diverse international projects and clients
Apply Nowđ February 17
Clinical Research Associate responsible for coordinating clinical trials at ICON plc. Ensuring compliance and analyzing critical data to maintain patient safety.