Clinical Trials Coordinator

Há 7 horas


São Paulo, São Paulo, Brasil beBeeResearch Tempo inteiro R$45.000 - R$75.000
Job Description

We are seeking a skilled Clinical Research Associate to manage global clinical trials. This role will involve both on-site and remote work, with opportunities to collaborate in a client-facing environment.

Main Responsibilities:
  • Serve as the primary contact for project teams and investigative sites, conduct site contacts, and document interactions for assigned sites according to study guidelines.
  • Monitor site performance and implement corrective action plans for sites not meeting expectations in collaboration with CRAs.
  • Assist CRAs with preparation for site visits, including data analysis and quality control of files.
  • Review Case Report Forms, generate queries, and resolve discrepancies against established data review guidelines.
  • Coordinate study visits and logistics, including shipment of trial materials, equipment, and laboratory samples.
Additional Tasks:
  • Liaise with project teams and other stakeholders to distribute and track clinical trial supplies.
  • Maintain activities after Site Activation, including updates to regulatory documentation.
  • Collaborate proactively with sites and project teams to ensure completion of maintenance tasks.
  • Demonstrate an understanding of clinical trial management systems (CTMS) and enter weekly details into CTMS or as required by the study.
  • Prepare Status Reports and assist with submissions and notifications to ethics committees and regulatory authorities.
Working Conditions:

This role offers flexibility between on-site and remote work, with opportunities to engage in client-facing collaborations.



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