Administrative Coordinator

Há 7 dias

São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro US$49.300 - US$64.100
Clinical Trials Assistant

Are you a detail-oriented and organized individual looking for a challenging role in clinical trials? Do you have excellent communication skills and experience working with clinical documentation?

About the Role

This Clinical Trials Assistant position involves performing daily administrative activities to ensure accurate Trial Master File delivery. You will assist Clinical Research Associates (CRAs) and Regulatory and Start-Up teams with updating and maintaining clinical documents, preparing and distributing clinical documentation, and managing Case Report Forms.

Key Responsibilities
  • Assist CRAs and RSU team with accurately updating and maintaining clinical documents and systems.
  • Prepare, handle, distribute, file, and archive clinical documentation and reports according to scope of work and standard operating procedures.
  • Assist with periodic review of study files for completeness.
  • Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Manage Case Report Forms (CRFs), queries and clinical data flow.
Requirements
  • Bachelor's degree or equivalent in a related field.
  • Previous experience working with CEP/CONEP.
  • Excellent computer skills, including Microsoft Word, Excel, and PowerPoint.
  • Strong written and verbal communication skills.
  • Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Benefits

Working with us means being part of a dynamic team that is passionate about improving patient outcomes. We offer a competitive compensation package, opportunities for career growth, and a collaborative work environment.

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