Klinikos – Expertise in Resourcing for Field Based Activities of a Clinical Trial in UK, Europe, North America, and Worldwide
Klinikos provides a niche service to Pharma, Bio-techs, Med-techs, and Academia where resourcing regulatory, project management, and monitoring/CRA expertise in Clinical Trials is a critical factor.
With over 20 years experience, Klinikos concentrates on Freelance Clinical Research Associate (CRA) and Regulatory (REG) requirements of global clinical studies.
For certain projects, you may have a freeze on head count resources but need the short-term or long-term assistance of clinical research personnel who are experienced and can step in with limited training and with a professional attitude to work with your clinical team. If that is the case, you may want to consider the use of Freelance Field-based Clinical Research Associates (CRAs) or Regulatory Specialists (REG) who have:
A breadth of study therapeutic experience
Having previously worked with pharma, CROs, Biotechs, Medtechs and Academia
Local Language
No communication breakdown
Local knowledge
Of regulatory requirements and good investigator sites
The ability to get started quickly
On your study without delays in training