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 you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.
Office-Based in St. Petersburg, Russia
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
QualificationsMD, College/University degree in Life Sciences or an equivalent combination of education, training & experienceIndependent on-site monitoring experience in RussiaExperience in all types of monitoring visits in Phase II and/or IIIMedical experience is a plusFull working proficiency in English and RussianProficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travel
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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