Administrative Coordinator

Há 2 dias

São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$45.679 - R$64.343

Job Overview:

">Clinical Trial Assistant 1
Perform daily administrative tasks in conjunction with the Clinical Research Associates and Regulatory teams to ensure a complete and accurate trial master file delivery.

">Essential Functions">
  • ">
  • Assist Clinical Research Associates (CRAs) and Regulatory teams with updating and maintaining clinical documents and systems that track site compliance and performance within project timelines.">
  • Assist the clinical team with preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.">
  • Assist with periodic review of study files for completeness.">
  • Assist CRAs and Regulatory teams with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.">
  • Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.">
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.">
  • May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.">
">Qualifications">
  • ">
  • High School Diploma or equivalent combination of education, training and experience.">
  • Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.">
  • Written and verbal communication skills including good command of English language.">
  • Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.">
  • Knowledge of applicable protocol requirements as provided in company training.">
"],

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