As a Senior Clinical Research Associate I 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.
Based in Kazakhstan
You will:
Conduct and report all types of 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
Qualifications
College/University degree in Life Sciences or an equivalent combination of education, training & experience
Independent on-site monitoring experience in Kazakhstan
Experience in all types of monitoring visits in Phase II and/or III, Oncology studies
Full working proficiency in English
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
Additional Information
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you
... the key support to clinical research projects, streamlining communication with medical ... sites participating in the clinical research projects Coordination of site-specific ... towards a career in clinical research, coordinating a variety of tasks ...
Компания: PSI CRO KazakhstanГород:Казахстан, Алматы, проспект Достык, 38
Зарплата:
от 400000 до 500000 KZT
Размещено:
almaty.hh.kz
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