Clinical Trial Associate

The Clinical Trial Associate will provide essential administrative and operational support to clinical research project teams, contributing to the successful execution of clinical trials. This role focuses on maintaining accurate trial documentation, coordinating project activities, and ensuring compliance with established quality standards. Working closely with Project Managers, Clinical Research Associates (CRAs), and other clinical operations professionals, you will help keep projects organized, efficient, and on schedule. You will play an important role in supporting document management, project tracking, and communication across clinical teams. This is an excellent opportunity to contribute to meaningful clinical research while developing your expertise in a collaborative, international environment.

• Bachelor's degree or equivalent professional experience, with at least one year of experience in a related administrative, clinical research, or project support role.

• Excellent written and verbal English communication skills, along with fluency in the language of the country where the position is based.

• Strong organizational and time-management skills, with the ability to manage multiple tasks and competing priorities independently.

• Exceptional attention to detail and a strong commitment to documentation accuracy, quality control, and compliance.

• Good judgment, problem-solving abilities, and the capacity to work independently while contributing effectively to a team.

• Proficiency in Microsoft Office applications, particularly Outlook, Word, Excel, and PowerPoint.

• Ability to collaborate with multidisciplinary teams and maintain effective communication in a remote working environment.