Обновлено 27 апреля№ 30901101
Вакансия в архиве
№ 30901101
27 мая
Этой вакансией интересовались сегодня 4 человека
Работа в Угличе / Вакансии / Клинические испытания / Специалист

Специалист по клиническим исследованиям

Москва
По договорённости, опыт работы от 1 года, полная занятость
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Обязанности:

Responsible for site feasibility, site selection and qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance to Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs) Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel Develop, review and edit clinical trial related documentation including but not limited to; Case Report Forms, Informed Consent Forms, study specific handbooks, guidelines and checklists. Perform pre-study initiation, interim monitoring and close out visits as required

Требования:

Medical Doctor (MD) degree or Pharmacist would be your advantage A minimum 2-year experience as a Clinical Research Associate Travel required Fluent in local languages of the countries under responsibilities and upper-intermediate English Thorough understanding of standard operating procedures, clinical research principles and process Energetic, active personality and ability to also work independently and to effectively prioritise tasks
  • • Высшее образование
  • • Английский язык (cвободное владение)

Условия:

Competitive compensation and benefit program Salary rate is under discussion Medical insurance Car allowance

Вакансия в архиве
№ 30901101
27 мая
Этой вакансией интересовались сегодня 4 человека

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