Clinical Support Trial Services

As the world of clinical research and clinical trials becomes more complex and regulated, budgets are getting tighter and workloads heavier. New European standards and processes, UK governance changes, the emphasis on data privacy and the impact of Covid globally, is creating a heightened sense of awareness within industry that we must move with the times and embrace these challenges.

It is apparent that like it or not, we all need to adapt to change and revise our working practices to ensure delivery and continued quality of new medicines and research. At Centrino we are fully aware of the need to constantly review our processes and ensure compliance and quality standards are always of paramount importance.

Independently we have been working with global pharmaceutical, biotech, and medical device companies since 1991. We have seen many changes during that time and have successfully built upon our experiences to forge strong, robust partnerships, a solid business model and emphasis on dependability.

Our therapeutic experience lies within all study phases of oncology, CNS, respiratory, infectious disease, cardiovascular, vaccines, osteoarthritis, dermatology amongst others. We are driven by our knowledge and experience of managing complex and challenging trials, and we want to share this expertise to help you get your study to the next phase.

Services We Provide

• Full clinical trial support including study set-up tasks (database design, ethics submissions, site selection, protocol writing, etc). Our project management team will be an integral part of your study, leading or supporting, with integrity and expertise. Our experience of working in different team environments, resolving issues, having the foresight to spot potential problems before they arise and working to resolve any challenging vendor relationships, are all aspects well-trodden by us.
• Full or partial project coordination, including site monitoring activities, CRA support, working with third-party vendors, data cleaning and review.
• Full feasibility services and informed consent form design process
• Electronic diary and data services in conjunction with one of our business affiliates
• SOP writing services and writing/review of all essential documents
• Assistance with TMF and eTMF design and implementation
• Exclusive access to our alliance pool team of expertise based in Belgium consisting of specialist doctors and active Investigators, working in several specialist therapy areas
• Biostatistical support and statistical reporting and analysis
• Coordination of Investigator meetings, SDV and full site selection process support
• Medical writing services to support protocol (and synopsis), investigator brochure, patient narratives, clinical study report, and more.

Project Resourcing/Recruitment

Tailor made clinical support services designed around your study

Centrino can assist your clinical study resource requirements, quickly and efficiently. As seasoned clinical program and project managers ourselves, we have a distinct and realistic approach to working with our clients and helping to shape what support is really needed. Unlike many other CROs, we will offer a completely bespoke service, providing support where you need it, and for precisely how long you need it for.

Resourcing engineered around you

If you need help during the last few weeks or months of a clinical study, we can provide project management and coordination to help you get over the final hurdle. We can help with study set-up, initiate sites, advise on TMF and eTMF procedures, write and review SOPs, provide data management support and even data entry. We could provide a handful of days a month or aim to fulfil whatever is required.