Clinical Research Associate /cardio


My client, one of the biggest CROs in Poland which carries out clinical research in Central & Western Europe is currently looking for an office-based Clinical Research Associate in Warsaw.

ONLY EXPERIENCED CANDIDATES WILL BE CONSIDERED

Summary of Job Specification:

Conducts site monitoring of clinical research studies according to Standard Operating Procedures and GCP Guidelines


Travel Required:
Available for travel from 50% to 80% of the time, including overnight stays as necessary, consistent with project needs and office location
Ability to drive and have a valid driver’s license

Education / Qualifications Required:
University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
Knowledge of GCP, monitoring procedures, basic understanding of regulatory requirements

Experience / Skills Required:
Minimum of two (2) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
Ability to monitor study sites independently according to protocol monitoring guidelines, SOP, GCP
Good planning, organization and problem solving abilities

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