Clinical Trials Manager

1 dia atrás

Rio de Janeiro, Rio de Janeiro, Brasil beBeeClinicalResearch Tempo inteiro R$64.000 - R$83.000
Study Coordinator Role Overview

The Study Coordinator provides essential support, facilitates daily clinical trial activities, and coordinates tasks in clinical research studies.

Key Responsibilities:
  • Supports Principal Investigators in conducting clinical trial projects, ensuring timely completion.
  • Compiles data, assists with preliminary analyses, and verifies accuracy.
  • Prepares progress reports and presentations as required by the project.
  • Coordinates administrative support functions for program activities, including data entry and document management.
  • Resolves data queries, oversees all aspects of assigned clinical trials from pre-study planning to successful completion.
Requirements:
  • Bachelor's degree in healthcare or a related field, with 3+ years of clinical trials experience.
  • Master's degree in healthcare or a related field, with 1+ years of clinical trials experience preferred.

This role demands exceptional organizational and analytical skills, strong written and verbal communication, and effective collaboration with multidisciplinary teams.

Competencies:
  • Advanced knowledge of administrative practices and operations.
  • Proficiency in computer software applications (Microsoft Office) and database management.
  • Expertise in quality improvement principles and methods.
  • Strong problem-solving and decision-making abilities.
  • Ability to maintain confidentiality and effectively communicate with diverse populations.

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