Global Oncology Trial Coordinator

Há 5 dias

São Paulo, São Paulo, Brasil beBeeResearch Tempo inteiro US$90.000 - US$120.000

Job Summary:

  • We are seeking a Clinical Research Associate III to assume the primary CRA role, conducting site visits and serving as the site manager.

Main Responsibilities:

  1. The selected candidate will perform and coordinate assigned aspects of clinical monitoring in accordance with Good Clinical Practices (GCPs) and Standard Operating Procedures (SOPs).
  2. Conduct site visits to determine protocol compliance and prepare required documentation.
  3. Develop collaborative relationships with investigative sites and study vendors.
  4. Provide training on protocols and studies to assigned sites.
  5. Track site performance metrics and provide oversight.
  6. Serve as mentor/trainer for less experienced CRAs.

Additional Accountabilities:

  1. Communicate site performance to the Clinical Study Team.
  2. Perform Serious Adverse Event reconciliation and resolve discrepancies.
  3. Collaborate with CST and clinical study sites to ensure timely delivery of study milestones.
  4. Attend regional investigator meetings and site booster visits.

Requirements:

  • Bachelor's degree in a relevant scientific discipline.
  • Minimum 3+ years of Clinical Operations experience and 2+ years of monitoring experience.
  • Experience in global oncology trials preferred.

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