Clinical Research Associate

A global, continuously growing, pharmaceutical company is looking to appoint a Clinical Research Associate (CRA) in Latvia, 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.

Job Description

  • Status

    Position has been filled

  • Posted

    10 years ago

  • Employment Type

    • Permanent (Full-time)

  • Function

    • Clinical Research

  • Industry

    • Pharmaceuticals

  • Therapeutic Area

    • Immunology

  • Seniority

    • Experienced

  • Location

    • Latvia

  • Eligibility

    • EU/EEA/EFTA citizenship or a current permit to work and reside in Latvia.

  • Recruiter

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.

Requirements

  • 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 Latvian, 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.