At QMED CRS, we are dedicated to providing exceptional support for global clinical trials and Investigator Initiated studies. We know that every research journey is unique and requires a personal touch, which is why we assign Clinical Research Coordinators (CRCs) to each research site with a focus tailored to individual protocols.
Our CRCs are more than just support staff; they are vital members of your research team. While they don’t conduct medical evaluations, their role is crucial in ensuring the smooth progress of your study. They assist with everything from participant recruitment and data collection to regulatory compliance and study logistics. Their goal is to make sure that every detail is handled with precision and care.
Each CRC at QMED CRS is a highly trained professional with extensive experience, bringing a wealth of knowledge and dedication to your project. With a strong emphasis on quality and ethical standards, our CRCs are committed to maintaining the integrity of your research and helping you achieve your study objectives.
Trust QMED CRS to provide the dedicated, knowledgeable support you need for a successful clinical trial. Together, we can advance research and improve outcomes with excellence and integrity.
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