Talent Bank - Russia - CRA / SCRA

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Sona***********

  • Russia
  • Last Update: 15.05.2019 at 12:00

Job Type
Full Time
Start
ASAP
Duration
6 Month +
Place
Moscow, RU
Country
Russia

Category


Clinical and medical development

Description


Responsibilities Of The Clinical Research Associate (CRA)
    • Perform all types of site visits (selection, initiation, interim and close out)
    • Work in accordance with company SOPs, GCP guidelines and country specific regulations
    • Site management activities to ensure adherence to protocol, SDV and CRF
    • Develop, collect, review and edit clinical trial documentation
    • Assist in protocol design as and when required
    • Ensure adequacy of drug shipment and drug accountability
    • Liaise and form positive working relationships with all colleagues, study site staff and sponsor representatives
    • Work closely and provide support to the study Project Manager
    • Organise and/or attend investigator meetings
Criteria
  • Bachelors degree level (or equivalent) within Medicine, Biological Sciences, Pharmacology, Nursing or relevant life science discipline
  • Significant experience within CRA role across a range of therapeutic areas
  • Work experience within a pharmaceutical company or CRO setting
  • Good working knowledge of ICH GCP and local regulatory requirements
  • Ability to independently perform all types of site visit (selection through to close out)
  • Fluency in English and Russian language (both written and spoken)
  • Willing and able to work site based 40%

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