Emerald Clinical
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.
Clinical Research Associate 2
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Emerald Clinical
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
• Coordinate investigator and site identification, feasibility assessment, and selection • Complete monitoring activities according to the Monitoring Plan and prepare monitoring visit reports • Plan, organize, conduct, and report site evaluation visits • Prepare and submit regulatory packages and Ethics Committee packages, including importation/exportation requirements • Negotiate site budgets and coordinate site contract execution • Track invoicing and ensure timely site payments • Plan, organize, and conduct site initiation visits • Develop and maintain monitoring tools and project-specific documents • Motivate and train investigators and trial site personnel on protocols, investigational products, and trial requirements • Collect, review, approve, and code essential trial-site documents for Trial Master File filing • Reconcile in-house Trial Master File and Investigator Site File contents • Coordinate distribution, tracking, handling, and destruction of investigational products and trial supplies • Maintain trial information in the clinical trial management system and tracking/reporting tools • Support strategies to boost recruitment efforts • Work within the Clinical Operations group to support site management, monitoring, trial implementation, regulatory compliance, and SOP adherence
🎯 Requirements
• Tertiary qualifications in a related science or health care discipline • More than 2 years’ experience in on-site monitoring and site management within an academic, CRO, or pharmaceutical environment • Experience in renal and/or oncology clinical trials is a plus • Practical knowledge of ICH-GCP guidelines • Knowledge of global and local ethical and regulatory research requirements • Competence in ethical and participant safety considerations • Competence in site start-up management • Competence in site conduct management • Competence in risk management • Competence in quality management • Competence in supply management • Knowledge of scientific concepts and clinical research design • Competence in issue escalation management • Competence in negotiation and conflict resolution • Critical thinking, problem-solving, decision-making, and strategic thinking skills • Solid interpersonal communication and presentation skills • Flexibility to work within a multidisciplinary team autonomously and with varied stakeholders • Ability to adapt to changing organizational priorities and ambiguous environments • Ability and willingness to travel
🏖️ Benefits
• 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 • Employee Wellbeing: Programs and initiatives designed to promote work-life balance, health, and team connection • Global engagement surveys • Recognition programs • Team-building events • Global Opportunities: Exposure to diverse projects and clients • Purpose-driven work contributing to clinical trials that improve lives • Collaboration and innovation in a global network
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