Study Operations Coordinator

Há 2 dias

Brasil beBeeClinical Tempo inteiro US$80.000 - US$95.000
Job Title: Clinical Study Team Assistant IDescription

This role is an integral part of the Core Study Team, responsible for providing operational support to ensure compliance with ICH-GCP and regulatory regulations. The Clinical Study Team Assistant will work closely with global study team members to manage tasks from start-up to close-out.

The key responsibilities include:

  • Providing study-level operational support to the Core Study Team
  • Management and oversight of Study Team shared spaces
  • TMF maintenance, compliance, and oversight
  • Management and oversight of Study Management Platform
  • Registry and/or Clinical Trial Management system(s) compliance and maintenance
  • Tracking and oversight of study level information
  • Liaising with cross-functional study team members
  • Quality Control (QC) of essential clinical trial documentation
  • Managing engagement of Independent Oversight Committees
Required Skills and Qualifications

To be successful in this role, you will need:

  • Proficiency in Microsoft Office applications
  • Relevant clinical research or clinical trial experience or relevant coursework
Benefits

This position offers a unique opportunity to work in a dynamic environment and contribute to the success of the Core Study Team. You will have the chance to develop your skills and expertise while working on complex projects.

Others

We are looking for a motivated and detail-oriented individual who can work independently and as part of a team. If you are passionate about clinical research and want to make a meaningful contribution, we encourage you to apply.

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