CLINICAL SERVICES

 

Clinical Operations department is one of the key divisions of LEGE ARTIS. Our major principle is conducting clinical trials “by the law of art“, that means strict adherence to the international standards in clinical research that are provided in our Standard Operating Procedures and Guidelines. Furthermore, we successfully exploit all benefits of the local environment.

LEGE ARTIS clinical team includes Project Managers, Clinical Research Associates (CRAs) and Clinical Research Assistants.

The Project Managers have overall responsibility for a project, including clinical, medical regulatory and financial aspects. The Project Manager coordinates the clinical team in cooperation with other departments in achieving the project objectives, whereas CRAs supported by Clinical Research Assistants mainly focus on clinical monitoring tasks.

 

CRA Team of Unique Experience

LEGE ARTIS CRAs are specialists with substantial medical, scientific and/or teaching experience that helped them in development their leadership, management and communication skills. They follow a strong project-based and results oriented approach, ensure consistent, accurate and timely management of the study process, and adhere to the highest ethical standards in clinical research. more>>>

 

What does “Clinical Trial Conduct” mean for LEGE ARTIS?

Routine clinical monitoring is the main part of a CRA’s work. However, in order to ensure the integrity of clinical trial processes at an investigational site level, clinical team members are normally involved in coordination and/or contribute to several other key activities. more>>>

 

Why LEGE ARTIS?

LEGE ARTIS clinical and medical teams have developed and utilize several specific techniques, including target sites selection, investigators trainings and site management that allow us to ensure adherence to the highest quality standards in clinical trials. more>>>