Senior Clinical Research Associate

Highly Competitive
  1. Permanent
  2. Clinical Research Associate (CRA)
  3. Russian Federation
Moscow, Russia
Posting date: 17 Sep 2020
31827

A Senior Clinical Research Associate is required at a truly global provider of strategic and operational services in safety reporting, medical information and regulatory affairs. This is an excellent job opportunity to join this company at their Moscow site.

Job Responsibilities

  • Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
  • Performs clinical study site management/monitoring activities in compliance with ICH
  • Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
  • Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, closeout visits
  • Communicates with investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.
  • Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.

Skills and Requirements

  • Min. 2 years of direct site monitoring experience in a bio/pharma/CRO.
  • No compromise on min monitoring experience however specific monitoring and therapeutic area experience
  • B.A./B.S. preferred with strong emphasis in science and/or biology

To Apply

In case you have difficulty in applying or if you have any questions, please contact Polina Sidorova at +44 0203 854 3535 or upload your CV on our website - www.proclinical.com.

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