Senior (5-10 ani)

<html><body>Join a leading global CRO as a Clinical Research Associate and play a pivotal role in managing and overseeing clinical trial activities. This is a fantastic opportunity to work one day per week onsite in Bucharest, ensuring trials are conducted in accordance with protocols, regulatory requirements, and industry standards.Key Responsibilities:<ul><li>Monitor clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</li><li>Conduct site visits to evaluate performance, address issues, and provide support for successful trial execution.</li><li>Collaborate with cross-functional teams to ensure accurate and timely data collection and reporting.</li><li>Provide training and guidance to site staff and fellow CRAs to uphold high standards of clinical trial conduct.</li><li>Build and maintain strong relationships with site personnel and stakeholders to facilitate smooth trial operations.</li></ul>Candidate Profile:<ul><li>University degree in life sciences, nursing, or medicine.</li><li>At least 2 years of experience in independent on-site monitoring of clinical trials.</li><li>Strong understanding of clinical trial processes and local regulatory requirements.</li><li>Willingness to travel extensively.</li><li>Proficiency in monitoring practices, data integrity, and site management, with expertise in clinical trial software and tools.</li><li>Excellent communication and interpersonal skills, with the ability to influence and drive compliance.</li></ul>Enjoy a competitive salary and the opportunity to work with a dynamic team in a supportive environment.</body></html>

Clinical Trial Coordinator

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