Clinical Research Associate


A global, continuously growing, pharmaceutical company is looking to appoint a Clinical Research Associate (CRA) in Lithuania, who will be responsible for all the aspects of clinical trial monitoring, from pre-study and initiation visits to maintenance of study files, routine monitoring and close-outs.

Company Offers

  • An attractive compensation package with benefits (company car, health insurance, performance bonus, etc.);
  • A new challenge and prospects of career progression within a growing company;
  • A high level of responsibility and independence;
  • A supportive and friendly working environment;
  • A flexibility to work from home.


  • University Degree (preferably in Life Sciences);
  • At least 2-3 years experience as a full-cycle clinical trial monitor (ideally with immunology studies);
  • Excellent communication and ability to work in cross-functional team;
  • Fluency in English and Lithuanian, both written and spoken. Russian would be an advantage;
  • Computer literacy (Microsoft Office tools);
  • Valid Driver’s license;
  • Prepared to travel locally and internationally (at least 50-60% of working time).

Main Duties & Responsibilities

  • Feasibility and Site Selection;
  • RA & EC Submissions;
  • Initiation and Monitoring visits;
  • Study Tracking and Close-outs.

Job Summary

This position has been filled
4 years ago
Employment Type:
Job Function:
Clinical Research
Seniority Level: