About us

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Yoshe Clinical   Operations limited is the UK-based Site Management Organisation. We support clinical trials with new medicines, for patients with various chronic diseases. Our experience includes Oncology, Virology, Cardiovascular, chronic pain and memory disorders resulting from inflammatory, neurological and neurodegenerative cond

Yoshe Clinical   Operations limited is the UK-based Site Management Organisation. We support clinical trials with new medicines, for patients with various chronic diseases. Our experience includes Oncology, Virology, Cardiovascular, chronic pain and memory disorders resulting from inflammatory, neurological and neurodegenerative conditions.

In addition, our clinical, IT and scientific specialists offer wide-ranging and practical expert advice to sponsors on their drug development programmes, based upon substantial experience in the public, private, academic and commercial   pharma fields.

Yoshe Clinical Operations has been ensuring clients in the biotechnology and pharmaceutical industries achieve their clinical research goals for over 8 years. As experts in the planning and delivery of clinical research, we understand the importance of time, cost and quality, and are able to guarantee these metrics are met. Yoshe offers a

Yoshe Clinical Operations has been ensuring clients in the biotechnology and pharmaceutical industries achieve their clinical research goals for over 8 years. As experts in the planning and delivery of clinical research, we understand the importance of time, cost and quality, and are able to guarantee these metrics are met. Yoshe offers a comprehensive portfolio of services which can be tailored to meet the individual needs of each client.

Yoshe Clinical Operations Clinical Development’s CRAs are based either regionally or in one of our five offices. This approach enables us to monitor in more than 5 countries of the world in a flexible and cost-effective manner.

As you would expect, our monitors are fully trained in GCP, the therapeutic area and the specifics of your stud

Yoshe Clinical Operations Clinical Development’s CRAs are based either regionally or in one of our five offices. This approach enables us to monitor in more than 5 countries of the world in a flexible and cost-effective manner.

As you would expect, our monitors are fully trained in GCP, the therapeutic area and the specifics of your study protocol. However, we also expect our CRAs to pro-actively manage their investigative sites.

Working closely with their study Project Manager, the monitors develop individual management plans for each of their centres – this includes a site-specific recruitment plan based on feasibility work.

Our CRAs also establish productive relationships with the Principal Investigator and other key players; they are responsible for ensuring that the activities of laboratories, pharmacists and other providers are fully integrated.