Covance Clinical Research Associates- CoSource Poland in United States

Job Overview



CRA II position available to work directly through our CoSource division with a large Pharmaceutical company in the cutting edge area of Oncology, specifically immunotherapy. As an experienced CRA you’ll be involved in initiation, routine & close out visits. Successful candidates will enjoy the benefits of working for a company that values a WORK / LIFE BALANCE!

Covance Poland is certified as “HR of the Highest Quality”, which confirms the highest standards of HR practices in our Company.

USPs of CRA II role:

  • Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit’ targets

  • Join a stable team of CRAs across and benefit from outstanding training and development, both initially and throughout your career

  • Join a company where people tend to stay for 6-10 years rather than 1-3!

  • Join a genuinely friendly and supportive company where they allow individuals to take ownership of their own performance.

  • ONCOLOGY Focussed

Other Information:

This role is a full time & permanent position employed through Covance.

Key words:

CRA II, GCP, Clinical Research Associate, Oncology, Warsaw, Poland, Clinical Monitor, Immunotherapy, Cancer Clinical trials

Education / Qualifications


  • Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines

  • Excellent understanding of Serious Adverse Event reporting

  • Fluency in English and Polish


  • Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in the Poland

Job Location(s) PL-Warsaw | PL

Job Number 2017-14261

Job Category Clinical Research Associate

Position Type Full-Time