A global CRO is looking to hire an experienced CRA to join them on a permanent basis. Working one day per week onsite in Bucharest, the successful candidate will play a critical role in overseeing and managing a sponsor's clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. Role Responsibilities: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Candidate Profile: University degree in a relevant field such as life sciences, nursing or medicine. Minimum of 2 years experience in independent on-site monitoring of clinical trials (experience in SSVs, SIVs, IMVs , COVs). Strong understanding of clinical trial processes and local regulatory requirements Willingness to travel 65- 75% of the time. Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. For additional information and a confidential discussion, please apply now with an updated CV.