Clinical Research Associate Site Manager

Há 3 dias


São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro R$74.400 - R$94.400

Clinical Research Associate Role Summary:

Fortrea is seeking a skilled Clinical Research Associate II to oversee site management for clinical studies and conduct site monitoring responsibilities.

The ideal candidate will have thorough knowledge of ICH GCP Guidelines, a strong understanding of local regulatory requirements, and excellent communication skills.

  • Key Responsibilities:
  • Manage sites for clinical studies according to Fortrea's Standard Operating Procedures and ICH GCP Guidelines.
  • Conduct site monitoring visits to ensure compliance with project plans and sponsor requirements.
  • Prepare and implement project plans related to Clinical Monitoring responsibilities.
  • Ensure data integrity by reviewing source documents and verifying data against established guidelines.

Requirements:

  • University or college degree in a related field or certification in an allied health profession.
  • Thorough understanding of ICH GCP Guidelines and local regulatory requirements.
  • Excellent communication and interpersonal skills.

Preferred Qualifications:

  • Working knowledge of Fortrea SOPs for site monitoring.
  • One or more years of experience in a related field.
  • Phase I monitoring experience.

Work Environment:

  • Standard office environment.
  • Clinical research unit and hospital environment (administrative only).
  • Risk of eye strain.


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