PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
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.
You will:Conduct and report all types of onsite monitoring visitsPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchSupport regulatory team in preparing documents for study submissions
QualificationsCollege/University degree in Life Sciences or an equivalent combination of education, training & experienceIndependent on-site monitoring experience in Czech RepublicExperience in all types of monitoring visits in Phase II and/or IIIExperience in Oncology is a plusFull working proficiency in English and CzechProficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travelValid driver’s license
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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