Klinikos - Provision of Freelance CRA & Clinical Investigator Sites in Europe

Klinikos is a European based niche service provider that concentrates on the key aspects of Site Management and monitoring to support Sponsors to initiate and complete clinical trials in the UK and Europe. We understand that each client has different needs and consequently our flexibility is crucial to your requirements.

Why use Klinikos?

With over 25 years of combined experience in the pharmaceutical industry the Klinikos principals have a broad and deep knowledge of the field of Clinical Research.

Freelance CRA Europe

We are a UK based clinical research company with proven experience in Investigator Site Management and the provision of Freelance CRA's throughout Europe
We have a gateway to Europe for accessing Clinical Research Associates (CRAs).

Klinikos - European Clinical Research Services

If you need a Clinical research company based in the UK with access to europe call Klinikos to discuss how we can help.
0141 952 1630

Let Klinikos determine and advise on the best site for your clinical trial.

Patient Recruitment Strategies for European Clinical Trials

Klinikos can deliver the right patient recruitment strategy for your UK and European clinical trial.

We provide experienced freelance CRAs throughout Europe.
If you are a Freelance CRA then contact us

Klinikos has a bank of Research Nurses in the UK available to assist your Investigator Sites.

Klinikos has successfully managed Investigator Sites from pre study selection through monitoring to close-down.

Look no further than Klinikos’s pre qualified Sites to save you time and money recruiting for your study.

Completion of Regulatory and ethics sumissions

Klinikos can advise and submit for both Regulatory and Ethics Approvals for your study in the UK.

Klinikos can conduct GCP training to help your Principal Investigators, Research Nurses, Study Site Co-ordinators and others.

CASE STUDIES

GCP Investigator Training

An NHS Client had identified clinical researchers in their Trust involved in phase II - III studies. On examination of the study site teams, it was evident that over 80% of the personnel had little or no GCP training and some sites had started recruitment.

TIPS & GUIDES

Download some free templates for use in clinical research trials and improve your efficiency.

LATEST BLOGS

UK as a Centre for Clinical Trials