Clinical Trial Monitoring Specialist

Há 4 dias


São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

About the Role

We are seeking a skilled Clinical Trial Monitoring Specialist to join our team at Thermo Fisher Scientific. In this role, you will be responsible for ensuring the quality and integrity of clinical trials through on-site monitoring visits and documentation.

Key Responsibilities

  • Conduct on-site monitoring visits to ensure compliance with protocols and regulations
  • Review and assess investigational products through physical inventory and records review
  • Document observations in reports and letters using approved business writing standards
  • Escalate observed deficiencies and issues to clinical management promptly
  • Participate in investigator meetings as necessary and help identify potential investigators
  • Ensure required essential documents are complete and in place according to ICH-GCP and applicable regulations

Requirements

  • Bachelor's degree in a life sciences related field or Registered Nursing certification equivalent
  • Minimal clinical monitoring experience comparable to 2 years in a clinical environment
  • Valid driver's license where applicable

Working Environment

Able to communicate and work effectively with diverse groups of people

Salary Range

$70,000 - $90,000 per year



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