Contract Research Organization

SMO services

Thank you for the possibility to introduce our SMO services that can provide the study centers with our competent study coordinators. We believe that they can bring benefit to all parties (CROs, sites and sponsors). In the current environment of “ A Risk-Based Approach to Monitoring” when off-site monitoring becomes more frequent way of monitoring, we can help you to achieve the effective way how to “manage the site” and how to deal with the requirements to reduce on site monitoring hours and keep the high quality and on-time entering of data at competitive costs.

We offer

Experienced and trained study coordinators that work in compliance with SOPs, Good Clinical Practices and ICH guidelines coordinate and administer research study associated activities, assist in project planning, ensures that the study protocol requirements are followed and maintain recordkeeping systems and procedures.

We provide SC with the following characteristics:

  • Bachelor degree equivalent or higher qualification within Nursing, Medicine or relevant Life Sciences.
  • Previous experience in a Clinical Research related role.
  • Proven track record of adherence to ICH GCP and applicable local regulatory requirements during the conduct of clinical trials.
  • Strong organisational and communication skills.
  • Fluent in English (both written and spoken).
  • Fluent in Slovakian and Czech (both written and spoken).

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