feedback

Clinical Research Associate II/III or Senior CRA

INC Research

Slovakia

A brief summary of duties you will be involved in as a CRA:

  • Site management and site staff performance including monitoring all types of clinical trials ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures;
  • Data Handling, Reporting and Tracking & administrative tasks;
  • Perform management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines.

Skills and attributes:

To succeed in this role you will need the following skills/experience:

  • Education - BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position;
  • Independent clinical monitoring experience;
  • Extensive understanding of SOPs, WI, FDA, and local regulations as well as ICH GCP guidelines;
  • Effective command of written and spoken English language.

For more details and to apply for this job click here

© EuroJobsites

This website uses cookies to make your experience better. Continued use of this website means you accept our cookie policy.  Accept Cookies