Klinikos - Provision of Freelance CRAs & 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 to manage your Clinical Trials?

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.

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Freelance Clinical Research Associates in Europe

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

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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
Clinical Trials Feasibility Assessment
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.

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

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

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

Selection of Investigators
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.

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

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Case Studies


Investigator Sites and Monitoring

Klinikos was asked to identify 35 GP Investigator sites in the UK as part of a Phase IV depression study throughout Europe for a Pharmaceutical Client and undertake the pre-study, initiation, monitoring and close down visits.

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

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