Site Operations Specialist

2 semanas atrás

São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro US$45.000 - US$60.000
Research Associate Specialist

This role involves overseeing clinical studies according to established standard operating procedures, international guidelines and applicable project plans.

Responsibilities include conducting site monitoring visits for clinical trials and ensuring compliance with regulatory requirements.

Key Responsibilities:
  • Manages site activities for clinical studies
  • Conducts site monitoring responsibilities for clinical trials
  • Prepares and implements project plans related to clinical monitoring duties
  • Verifies adherence to informed consent procedures and protocol requirements
  • Ensures data integrity by reviewing source documents, generating queries and resolving discrepancies against established guidelines
  • Confirms completeness and currency of site regulatory documents and sponsor records throughout the trial duration
  • Guarantees accurate investigational product inventory and secure storage per protocol requirements
  • Ensures quality control and CRA performance metrics are met
  • Maintains audit readiness at the site level
  • Assumes lead CRA responsibilities as assigned

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