Accessability Links
Cookies on our website
By continuing to use this website we will assume you are happy to receive cookies as outlined in our cookie policy
Accept Policy

CRA II

Moscow
Permanent
Reference: JR061800_1573822808
Description

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Clinical Research Associates (CRA's) identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV ensuring adherence to applicable regulations and principles of ICH-GCP.

Overview of the Role

  • Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
  • Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.

Role Requirements

  • With a University degree in medicine, science, or equivalent
  • You should also have knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
  • You will possess excellent written and verbal communication in English and local language
  • Good interpersonal skills enabling you to deal with queries in a timely manner
  • You must be available to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving licence
Similar jobs
CRA II

Moscow

Permanent

View Job Shortlist

CRA II

Moscow

Permanent

View Job Shortlist

CRA II

Moscow

Permanent

View Job Shortlist

Study Start Up Manager

Moscow

Permanent

View Job Shortlist

 

Back to Top