Clinical Lead | Clinical Trial Manager

pAbout the Company Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world's top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end‐to‐end clinical trial solutions across all phases, offering Phase I-IV and real‐world studies. With over 25 years of experience and a world‐renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality. Our 800+ employees across Asia‐Pacific, Europe, and the Americas are embedded in communities worldwide, driving faster recruitment, deeper patient engagement, and meaningful results that move medicine forward. /ppAbout the Role We are seeking an experienced Clinical Lead to join our growing team in Europe. This home‐based role offers flexibility while providing the opportunity to lead global and regional clinical trials across multiple therapeutic areas. The ideal candidate will have experience managing clinical trials and a strong background in project leadership, clinical operations, and strategic trial execution. /ppYour Responsibilities /ppOversee clinical trials, ensuring successful execution from start‐up to close‐out. /ppLead site selection and feasibility assessments, working closely with CRAs and investigators. /ppManage study timelines, budgets, and deliverables, ensuring adherence to project objectives. /ppProvide oversight on protocol administration, site initiation, monitoring, and study progress. /ppCollaborate cross‐functionally with internal and external stakeholders, including sponsors, investigators, and project teams. /ppEnsure compliance with GCP, FDA regulations, and company SOPs. /ppTrain and mentor CRAs and site staff, ensuring protocol adherence and data integrity. /ppAbout You /ppRenal experience is mandatory. /ppBachelor's degree in a science‐related field (RN preferred) with industry experience, including 1‐2 years as a Clinical Trial Manager/Clinical Lead. /ppStrong background in monitoring and site management, preferably with experience in oncology or other complex indications. /ppCCRA or CCRP certification is strongly preferred. /ppExcellent knowledge of GCP, FDA regulations, and clinical trial best practices. /ppAbility to manage multiple projects, timelines, and stakeholders efficiently. /ppStrong leadership, problem‐solving, and communication skills. /ppWillingness to travel up to 20% as required. /ppWhy Join Us? At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. Joining our team means being part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide. /ppHere's What Makes Us Stand Out /ppPurpose‐Driven Work: Contribute to clinical trials that genuinely improve lives, focusing on therapies in renal, cardiometabolic, and oncology. /ppGlobal Reach, Local Expertise: Teams connect with local communities, building trust and meaningful engagement for every trial. /ppCollaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges. /ppWhat

We Offer
/ppCompetitive Compensation: A tailored salary and benefits package. /ppFlexibility: Hybrid or remote working arrangements, depending on your location and role. /ppCareer Growth: Access to learning opportunities and a global network of scientific leaders. /ppEmployee Wellbeing: Programs and initiatives to promote work‐life balance, health, and team connection. /ppGlobal Opportunities: Exposure to diverse projects and clients. /ppWe are an equal‐opportunity employer and encourage applications from all qualified candidates. /p