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.
Hybrid role in Kyiv, Ukraine
You will:
Conduct and report all types of onsite monitoring visitsBe involved in study startupPerform 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
Qualifications
MD, PharmD or MSc2+ years of independent on-site monitoring experience in UkraineExperience in all types of monitoring visits in Phase II and/or IIIExperience in Oncology/Ulcerative Colitis/Antibiotics trials is a plusFull working proficiency in English and UkrainianProficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travel
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.
Job DescriptionAs a Clinical Research Associate at PSI, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic ... monitoring visits in Phase II and or IIIExperience in Oncology ... become an expert in clinical research.
Компания: PSI CROГород:, Kyiv,
Зарплата: Размещено:
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