Highly rated by CROs & Sponsors |. 
4.2 / 5 stars
One integrated suite for maximum control over clinical research for CROs and sponsors
ResearchManager Clinical Research Suite supports Clinical Operations and Clinical Data Management within one modular environment. Designed for sponsors and CROs who want to operate scalably without losing control.
- From study design to closeout and archiving
- Integrated technology and professional support
- One consistent environment for execution, data and governance
Fully compliant with relevant laws and regulations
Control becomes complex once multiple parties work together
Initiating and managing clinical trials is complex, especially when CROs, sponsors and sites are working with different or poorly integrated systems. This often leads to inefficiencies, errors and delays.
Avoid fragmentation and lack of overview and control
Fragmented data, documents and progress make it difficult to maintain a grip on insight, control and collaboration. The Clinical Research Suite brings everything together in one central environment with real-time dashboards. With clear roles and access rights, teams always maintain full visibility and control.
Reduce risk of error and pressure for compliance
Manual data transfer, duplicate entries and fragmented audit trails increase risk in inspections and audits. With the Clinical Research Suite, these problems are a thing of the past: integrated audit trails, automatic validations and streamlined workflows prevent errors and ensure you’re always audit-ready.
Fewer restrictions, more flexibility
Scaling up to multiple studies or modifying processes is time-consuming with separate systems. The Clinical Research Suite makes this efficient and error-free thanks to reusable templates, standardized workflows and centralized documents, allowing new studies to be set up quickly and processes to be modified easily.
From slow study start-up to fast time-to-market
Slow configuration, manual workflows and lack of visibility often delay study start-up and execution. With reusable templates, automated reporting and streamlined workflows in Clinical Research Suite, studies can be started faster and completed efficiently, significantly reducing time-to-market.
Our promise
At ResearchManager, we believe that the Clinical Research Suite delivers value only when the setup is right. That’s why we configure the initial study together as part of the implementation, without additional consulting fees.
- A setup aligned with organization, governance and roles
- Directly in line with the study protocol
- Deployable to teams and sites from day one
- Scalable with growing study volume
This creates not only a platform, but a stable basis for control and continuity.
Transparent and scalable pricing model
Our pricing structure is based on the number of studies, not users or data volume.
✓ Transparent ✓ Predictable ✓ Geared for growth
On Demand
- Suitable for flexible or project use.
- License fees apply only during active studies.
- No ongoing charges when no study is in progress
Enterprise
- For CROs and sponsors with continuous study volume.
- A fixed license fee, tailored to the number of studies.
- Predictability and budget certainty with structural growth.
Satisfied users of our platform
For over 13 years, CROs & sponsors have relied on the Clinical Research Suite to conduct clinical research in a structured and reliable way. Discover how we help organizations run studies more efficiently, compliantly, and with full control.
Thierry Wetting
Global Sales Manager - CROs & Sponsors
Steafan McLaverty
Account Manager
Curious about the possibilities?
Our team is happy to think with you about which tools fit your personal situation. Request a quote or feel free to schedule an meeting.
