Clinical Site Quality Specialist

Há 6 dias


São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$69.173 - R$98.218
Clinical Research Associate Role

Job Summary:

This role involves managing site quality and delivery from site identification through close-out as the direct point of contact for clinical sites.

  • Build relationships with sites to ensure successful initiation, patient recruitment, and compliance with regulations.
  • Evaluate site efficacy, assess compliance, and develop strategies for improvement.
  • Oversee trial conduct at designated sites, ensuring subject rights and data integrity.
Key Responsibilities

The Clinical Research Associate will be responsible for:

  • Managing site performance, including problem-solving and issue resolution.
  • Developing and implementing patient recruitment strategies.
  • Ensuring compliance with GCP and regulatory requirements.
Required Skills and Qualifications

To succeed in this role, you will need:

  • Site management experience or equivalent experience in clinical research.
  • A strong understanding of clinical trials methodology and terminology.
  • Advanced communication and problem-solving skills.
Benefits

This role offers a range of benefits, including:

  • Opportunities for professional growth and development.
  • A dynamic and supportive team environment.
  • The chance to work on diverse projects and contribute to innovative solutions.
About the Role

This is an exciting opportunity to join our team and make a meaningful contribution to the field of clinical research. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply.



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