Stellendetail

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:

• Monitor clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conduct site visits to evaluate performance, address issues, and provide support for successful trial execution.
• Collaborate with cross-functional teams to ensure accurate and timely data collection and reporting.
• Provide training and guidance to site staff and fellow CRAs to uphold high standards of clinical trial conduct.
• Build and maintain strong relationships with site personnel and stakeholders to facilitate smooth trial operations.

Candidate Profile:

• University degree in life sciences, nursing, or medicine.
• At least 2 years of experience in independent on-site monitoring of clinical trials.
• Strong understanding of clinical trial processes and local regulatory requirements.
• Willingness to travel extensively.
• Proficiency in monitoring practices, data integrity, and site management, with expertise in clinical trial software and tools.
• Excellent communication and interpersonal skills, with the ability to influence and drive compliance.

Enjoy a competitive salary and the opportunity to work with a dynamic team in a supportive environment.