Pharmacovigilance Specialist

з/п не указана

Вакансия в архиве

Работодатель, вероятно, уже нашел нужного кандидата и больше не принимает отклики на эту вакансию

Показать описание вакансии

Требуемый опыт работы: не требуется

Проектная/Временная работа, полный день

Pharmacovigilance Specialist (temporary position)

Our Client is one of the largest pharmaceutical companies in the world is looking for Pharmacovigilance Specialist - temporary position.

Responsibilities

  • translation and information processing of spontaneous reports of adverse reactions that emerged during clinical trials
  • entering this data to the global database security
  • forward this data to the appropriate center, which is responsible
  • сomparing of reports of adverse reactions received from other units
  • submission to the local regulatory authorities, if required, safety reports of individual spontaneous cases of adverse reactions that emerged during clinical trials
  • documentation, storage and archiving
  • compliance with all standards of pharmacovigilance and local policies / procedures on safety
  • assistance in training for the staff of the pharmacovigilance

Requirements

  • Fluency in English
  • experience in a pharmaceutical company in the department of clinical trials or medical department - would be a plus
  • accuracy and precision, attention to detail
  • motivation and interest to work with the processes and procedures to comply with all nuances

Working conditions:

  • The contract for 5-6 months
  • Employment - full rate
  • Official employment
  • Training in all procedures

If you are interested in this vacancy, please send your CV.

 Доступно соискателям с инвалидностью 

Ключевые навыки

Clinical ResearchGCP (Good Clinical Practice)Documentary

Адрес

Площадь Льва Толстого, Киев, Владимирская улица, 77А
Показать на карте
­
Написать сопроводительное письмоПисьмо отправлено

Сопроводительное письмо к отклику

Вакансия опубликована 6 октября 2016