Clinical Research Associate II
PSI CRO
Prague, Prague, Czech republic
před 2 hodinami
Job Description

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Office-based

You will:

  • Conduct and report SIV, RMV, COV onsite monitoring visits
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions
  • Prepare and particiapte on audits and inspections

Qualifications

 

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • At least 2+ years of independent on-site monitoring experience in Czech Republic
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in Oncology or Hematology or Gastroenterology therapeutic indications is a plus
  • Full working proficiency in English and Czech
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel
  • Valid driver’s license

 



Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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