Clinical Trial Management Services

Services built around your needs

During any stage of a clinical trial, you need reliable project managers, access to specialist resources and end-to-end collaboration. Simbec-Orion provides it all.

As an experienced CRO, we offer full clinical trial management services from patient recruitment and pharmacovigilance, through to laboratory services and data processing.

We are a full-service CRO. Whether it’s early phase, phase II or phase III, we can design and deliver clinical development projects shaped around your unique requirements. We build a relationship with our clients to understand your limitations, goals and timelines for a reliable, comprehensive and attentive service.

Ready to collaborate?

Reducing risk

Vaccines, new chemical entities (NCEs), small molecules, biologics, gene therapy. Our experience spans all product types and we understand clinical development in challenging therapy areas. By putting patients first, we reduce the risks of recruitment and retention, and mitigate delays with regulatory authorities.

Working with unique challenges

We’ve encountered many unique challenges that hinder complex hospital-based studies, including rare diseases and oncology trials. But as a full-service CRO of our size, we’re ideally placed to meet them head-on. We maximise site selection, form close links with patient advocacy groups, and enrol patients. We overcome hurdles to help you get medicines to market.

Effective site management

Our clinical trial management services cover the full scope of your project, including site management. Not only will you have a dedicated Project Manager, but our Clinical Research Associates (CRAs) are decentralised, meaning that they are located close to clinical sites. This facilitates close communication, driving patient enrolment and ensuring effective site management.

Reliable clinical data

Not only can we facilitate effective and cost-efficient clinical trials, we also process and manage data accurately using our internal management systems. With accurate and adaptive biometrics services, we can conduct statistical analysis, planning and reporting. We put together a quality biostatistical framework suitable for presenting to regulatory bodies. Find out more about our clinical trial data management services.

Clinical trial services that drive results

We’re a low hierarchy operation and we believe in getting the job done efficiently and with transparency. Your dedicated project manager will drive the project from start to finish, and you’ll have access to the senior management team for face-to-face troubleshooting.

Responsive and adaptable

With strong governance and project escalation communication plans in place from day one, we mitigate risk and work around any obstacles that may arise. We understand that complex studies evolve and may require a change in scale or flexibility. When your study needs it, you’ll find our team to be responsive and have the experience to handle any challenges that may arise.

Meeting project milestones

Our clinical trial management services are designed for small to medium drug developers. We understand the importance of meeting milestones to secure investor confidence and additional funding for clinical development. Our agile set-up means we can flex resources to shorten timelines and remove bottlenecks. You can provide data to support your major milestones.

Discover how we have delivered challenging clinical trials

Fabrice Chartier, CEO

Discover how our team can work with you to provide innovative solutions to the most challenging clinical trials – in the most efficient and cost-effective way.

Let’s collaborate

If you think we could be right for you, get in touch.

Submit an RFI/RFP

Simbec-Orion was able to complete a European phase 2a study in record time, thanks to efficient study management and a great commitment from everyone within the organization.

Paul Gineste, Abivax