For Hospitals & Sites

MCR Clinical Site
Manager™ (CSM™)

For Centers conducting clinical trials

What is MCR Clinical Site Manager™ ?

MCR Clinical Site Manager™ is a system for site managers and study coordinators to efficiently contract, supervise and bill. 

It is one of three systems developed by MCR Clinic™ for clinical trials. 

These systems not only do not interfere with existing systems used in hospitals, but they also do not interfere with the existing systems.


All MCR Clinic™ systems share the same communication module with dynamically generated forms, allowing site, sponsor, CRO and technical support staff to efficiently contact, notify and remind you of issues.

Most study or subject information and data is automatically generated or appended to the message, making communication faster, more user-friendly, error-free and adding another layer of data security.

Benefits for you and your facility

MCR Clinical Site Manager™ (CSM™) addresses common concerns

Knowledge in one place #allinone

Ensure consistency of management, medical, financial information about your clinical trial.

Contracting of services

Automate the process of creating the study plan and price list together with the sponsor/CRO.

Maximise trial budget

Ability to renegotiate and update the price list during the trial.

Eliminate facility financial losses

Accurate billing for medical services provided.

Accelerate settlements with sponsor/CRO

Improved financial liquidity of the site.

Full financial control

Checking procedures on an ongoing basis, access to current documentation at each stage of the study.

Other MCR CLINIC™ systems

MCR eSource Remote Viewer™ (eSRV™)

System for remote monitoring of studies in the hybrid model for sponsors and CRO companies.

MCR Data Communication Integrator™ (DCI™)

System for secure and automated data exchange between different systems used in clinical trials.

Security of MCR Clinic™ systems

Proven in real-world environments

MCR Clinic™ systems have been tested in oncology trials conducted at university teaching hospitals in collaboration with leading pharmaceutical companies.

Conforms to national and international standards

MCR Clinic™ systems are designed to operate in accordance with the Regulatory Model based on regulations and guidelines concerning both clinical research, personal data protection and healthcare information system.

Meet the highest IT requirements

MCR Clinic™ systems meet the highest medical IT requirements in Cloud and Software-as-a-Service infrastructure (Microsoft Azure, FHIR Fast Healthcare Interoperable Resource, HL7 CDA and higher for medical data storage and exchange).

Email or call to schedule a meeting

Krystyna Antolak

+48 789 229 070

k.antolak@mcr.clinic

Anna Urban-Marcinkiewicz

   +48 789 266 610    

a.marcinkiewicz@mcr.clinic