Senior Clinical Trial Coordinator

Há 7 dias

São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$40.000 - R$60.000

Job Overview

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  • Support Clinical Research Associates and Regulatory Teams">
  • Assist with Trial Master File Delivery">
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The role involves daily administrative activities to ensure the delivery of a complete and accurate Trial Master File.

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Key Responsibilities:

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  1. ">
  2. Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team in updating and maintaining clinical documents and systems that track site compliance and performance within project timelines.">
  3. Collaborate with the clinical team on preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to standard operating procedures.">
  4. Review study files for completeness.">
  5. Coordinate the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.">
  6. Act as a central contact for clinical team communications, correspondence, and associated documentation.">
  7. Mentor less experienced Clinical Trial Assistants (CTAs).">
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Requirements:

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  • ">
  • Bachelor's degree or equivalent.">
  • 5 years' experience in administrative support.">
  • Proficiency in Microsoft Office applications.">
  • Strong written and verbal communication skills.">
  • Ability to establish effective working relationships.">
  • Knowledge of Good Clinical Practice (GCP) guidelines.">
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About This Role

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This is an exciting opportunity to work in a dynamic environment and contribute to the success of our organization.

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We offer a competitive salary and benefits package.

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How to Apply

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Please submit your application, including your resume and cover letter.

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