Clinical Research Associate

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.