Clinical Research Associate/Senior Clinical Research Associate

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Требуемый опыт работы: 1–3 года

Полная занятость, полный день

OCT is a leading CRO operating in Russia, Central and Eastern Europe and the US announces an opening of a Clinical Research Associate office-based in St.Petersburg.

This position presumes primarily responsibilities of monitoring (pre-study, initiation, routine, and close-out visits) of investigator sites for the compliance to the study protocol, ICH GCP, company’s SOPs and applicable regulations.

Job responsibilities:

  • Conduct and reporting of pre-study, initiation, routine monitoring and closeout visits
    Communication with investigational sites and sites management
  • Ensuring the integrity of clinical data in adherence to all applicable regulatory guidelines, company’s SOPs and project-specific operating procedures
  • Assistance in feasibility studies
  • Negotiations of clinical trials agreements with the investigator sites and study budgets
  • Obtaining and review of required study documents from investigational sites
  • Project-specific training of sites and teams


  • MD or University degree in Life Sciences
  • Fluent English, written and spoken
  • Sound management skills
  • Effective oral and written communication kills
  • Demonstrated computer skills (MS Office Applications)
  • Minimum a year of independent monitoring experience in clinical trials.
  • Ability to travel at least 60-65% of working time

We offer:

  • Challenging job in a highly qualified team
  • Employee-friendly work environment
  • Competitive salary
  • Professional growth in clinical research field


Санкт-Петербург, Ковенский переулок, 5
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Вакансия опубликована 13 августа 2019 в Санкт-Петербурге

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