Clinical Research Associate - Talent Pipeline Opportunity

Clinical Research Associate - Talent Pipeline Opportunity Who We Are 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. Global Expertise. Local Insight. Real Impact. Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes. Our 800+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward. About the Role Emerald Clinical Trials is building a pipeline of talented Clinical Research Associates across the United States as we prepare for continued growth and future study awards. This posting represents an opportunity to join our future talent community. Hiring timelines may vary and successful applicants may experience a delay in communication while studies progress through contracting and award stages. Your Responsibilities Conduct qualification, initiation, monitoring, and close-out visits. Ensure patient safety, protocol compliance, and data integrity. Review source data and study documentation. Support site activation and study conduct activities. Build strong relationships with investigators and site personnel. Contribute to recruitment and retention initiatives. Maintain accurate documentation and reporting in accordance with company requirements. Escalate study risks and issues appropriately. About You Bachelor's degree in a scientific or healthcare discipline. Minimum 2 years of on-site monitoring experience. Strong understanding of FDA regulations and ICH-GCP. Proven site management experience. Excellent organizational and communication skills. Ability to travel extensively throughout assigned regions. Experience within renal, nephrology, rare disease, cardiometabolic, or oncology studies is preferred. Why Join Us? At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first - both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide. Here’s what makes us stand out: · Purpose-Driven Work : You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology. · Global Reach, Local Expertise : Our teams connect with local communities, building trust and meaningful engagement for every trial. · Collaboration and Innovation : Work in a culture that values diverse perspectives and creative solutions to solve global health challenges. What We Offer We understand that great work happens when people feel valued and supported. That’s why we provide: · 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. Interested? Apply now and help us achieve our mission to improve the health of millions worldwide. We are an equal-opportunity employer and encourage applications from all qualified candidates. The expected salary range for this position is $110,000 - $130,000 per year, depending on experience and qualifications. Department Clinical Operations Role Clinical Research Associate 2 Locations United States Remote status Fully Remote