As part of our strategic partnership, we will carefully assign a CPM perfectly suited to helping you overcome your challenges.

Caico Medical has around 10 CPMs that works internationally in studies performed in Europe and beyond. The CPM team has  a long track record of reliable support (i.e., 113 years cumulative clinical experience) for a  diverse range of projects regardless of their size, therapeutic area, or complexity.

A highly skilled Clinical Project Manager (CPM) is a pre-requisite for a successful clinical study. Our CPMs are extensively trained and competent, with experience in managing cross-functional teams executing international Phase I-IV studies as well as medical device/IVD studies from initiation to completion.

The CPM will act as main point of contact internally and externally. They will always work to make sure that deliverables are completed with high quality, on budget and time as well as to the customer’s satisfaction.

Our CPMs can also be outsourced for your specific needs.

To ensure the success of your clinical study, our CRAs work closely with the sites to make sure that the study protocol is followed, informed consent is correctly obtained, adverse events are reported, relevant records are maintained and study drug or devices are accounted for and reconciled.

Caico Medical has CRAs in 6 countries and can perform local monitoring in the following countries; Norway, Sweden, Denmark, Finland, UK, Germany, Austria,  Switzerland and in the Netherlands.

Our CRAs are an essential part in developing a good working relationship with the site and the project manager through active communication and support throughout the conduct of a clinical study.

The Study Start-up phase is an important part of clinical studies to reach important milestones such as first subject enrolled. Our CRAs in close collaboration with our Start-up group are always involved at an early stage of the study. They perform activities as local regulatory, ethics submissions and other required local submission (such as Biobank), site contract and budget negotiations and together creating a good collaboration with the sites from an early stage.

All members of our clinical operations team have extensive experience in running clinical studies and are in addition regularly trained in ICH-GCP/ISO 14155/20916, SOPs, guidelines, policies and practices to ensure studies are implemented and followed up with high quality.

Our global reach with local presence and offices result in good oversight, training and management of the team. We involve a local CRA from feasibility/selection up to the end of the study – leading to one main point of contact for the site.

Our CRAs can also be outsourced to you for your specific needs.

Finding the right sites and investigators is key to your study success. With our large network of trial infrastructure and first hand experience with the sites, we can ensure that the right site is identified for your study based on your needs and project criteria. We offer great flexibility and have the ability to perform feasibility with short notice without loss of quality.