(Jr) Clinical Research Associates – Top Global CRO / Moscow, St. Pete or Novosibirsk, Russia

My Client is a predominant name within the drug development sector with and outstanding reputation for delivering clinical research on a global scale. Due to acquisition of new projects, they are looking for Clinical Research Associates at different levels – from Jr CRA to Sr CRA to be based either in one of their offices in Russia or to work from home.

Responsibilities:

  • Site monitoring including close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties
  • Site and registry management as prescribed in the project plans
  • Organising and making presentations at Investigator Meetings
  • Participation in the development of protocols and CRFs
  • Liaising with CPM to evaluate needs, resources and timelines

Requirements:

  • Minimum 1 year of experience in monitoring clinical trials
  • Excellent site monitoring and site management skills and understanding of SAEs
  • Degree or equivalent  in a life science discipline
  • Fluency in Russian and English

To apply for this role, please send your CV to anna@pharmaprofessionals.eu

(Jr) Clinical Research Associates – Top Global CRO / Moscow, St. Pete or Novosibirsk, Russia was last modified: August 24th, 2017 by Admin