Experienced Clinical Research Associate Sponsor-dedicated - Riyadh
منذ شهر

Job summary:
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol.
وصف الوظيفة
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احصل على الوصول الكامل إلى جميع الوظائف الرفيعة المستوى واحصل على وظيفة أحلامك.
وظائف مماثلة
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. · ...
Perform site monitoring visits according to contracted scope of work and Good Clinical Practice. · Work with sites to adapt subject recruitment plan in line with project needs. · Evaluate study site practices related to protocol adherence. · ...
+ Manage cross-functional project teams + Develop integrated study management plans + Ensure financial success of projects + Forecast opportunities to accelerate activities Job Overview · ...
Perform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery. · Assist CRAs and RSU team with accurately updating maintaining clinical documents systems ...
Perform daily administrative activities in conjunction with Clinical Research Associates and Regulatory teams to ensure complete Trial Master File delivery. · ...
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