Clinical Research Assistant

Há 18 horas


Rio de Janeiro, Rio de Janeiro, Brasil beBeeStudy Tempo inteiro R$64.800 - R$85.200
Job Summary

The Study Coordinator plays a pivotal role in facilitating daily clinical trial activities, collaborating with Principal Investigators to ensure compliance with federal regulations and university policies.

Key Responsibilities
  • Assist Principal Investigators in conducting various clinical trial projects, compiling data, and performing routine preliminary analyses.
  • Work under the guidance of the Clinical Trials Senior Lead Study Coordinator, preparing progress reports, presentations, and coordinating administrative support functions.
  • Coordinate all aspects of assigned clinical trials from pre-study planning through successful completion, including patient monitoring and quality control review of source documents.
  • Monitor patients throughout the active treatment phase, reporting Adverse Events (AEs) and Serious Adverse Events (SAEs) to the PI and Clinical Trials Senior Lead Study Coordinator.
Requirements
  • Bachelor's degree in healthcare or related field and 3+ years of clinical trials experience.
  • Master's degree in healthcare or related field and 1+ year of clinical trials experience preferred.
Benefits

This position offers an opportunity to work in a dynamic research environment, collaborating with multidisciplinary teams across departmental lines. The ideal candidate will possess excellent written and verbal communication skills, strong organizational and analytical abilities, and the ability to exercise discretion and maintain confidentiality.



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