Clinical Research Lead

2 semanas atrás

São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$80.000 - R$120.000
Job Title: Clinical Research Lead

The Clinical Research Lead will oversee the execution of clinical trials at assigned sites, ensuring timely and accurate data collection. The successful candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines and experience in implementing risk-based monitoring models.

In this role, you will be responsible for site feasibility assessments, investigator meetings, and executing activities within site initiation, start-up, preparation, and conduct of site monitoring. Additionally, you will contribute to site-level recruitment strategies and contingency planning, ensure site study supplies are adequate, and accurately document clinical drug supplies and returns.

You will work closely with internal stakeholders to ensure Corrective Action Preventative Action (CAPA) is completed for Quality Assurance (QA) site audits and quality issues identified at the site. You will also prepare trial sites for close-out, conduct final close-out visits, and establish and maintain good working relationships with external partners.

To succeed in this position, you should possess excellent communication and project management skills, with the ability to prioritize tasks and meet deadlines. Experience with electronic data capture systems and audit trail software is highly desirable.

Key Responsibilities:

  • Execute site initiation, start-up, preparation, and conduct of site monitoring
  • Contribute to site-level recruitment strategies and contingency planning
  • Ensure site study supplies are adequate and accurately document clinical drug supplies and returns
  • Prepare trial sites for close-out and conduct final close-out visits

This is an exciting opportunity to work in a dynamic environment and contribute to the success of our clinical trials. If you have a strong passion for clinical research and excellent leadership skills, we encourage you to apply.

Key Qualifications:

  • Bachelor's degree in a related field
  • Minimum 5 years' experience in clinical research
  • Strong knowledge of GCP guidelines
  • Experience with electronic data capture systems and audit trail software
  • Excellent communication and project management skills

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