Clinical Research Associate
Pubblicato il 29-08-2026 - Altro in Roma
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 expanding its European talent network and is seeking experienced Clinical Research Associates (CRA II and Senior CRA level) for future opportunities.
This is a pipelining position. Applications will be reviewed as new projects and resource requirements emerge. There may be a delay in progressing candidates through the hiring process depending on study awards and business needs.
Your Responsibilities
Conduct site qualification, initiation, routine monitoring, and close-out visits.
Ensure protocol compliance and patient safety.
Review source documentation and validate study data.
Support investigator sites throughout the clinical trial lifecycle.
Manage site relationships and provide training as required.
Ensure timely issue identification and escalation.
Maintain high-quality documentation wit