Oncology Monitoring Specialist I/II

2 weeks ago


Los Angeles, California, United States ICON Strategic Solutions Full time

Essential Qualifications:

Minimum of 1 year of independent onsite monitoring experience is required.

Oncology expertise is mandatory.

  • Engages in multiple clinical trials within the Oncology sector.
  • Focuses on quality of life with regional travel responsibilities.
  • Exhibits leadership qualities by participating in specific initiatives as necessary and serving as a Subject Matter Expert (SME) for systems and processes.
  • Mentors and coaches junior flexible team members.
  • Assumes the role of Lead Study Manager, providing training to other Study Managers on the project.
  • Prepares site initiation documents for studies, including the Site Initiation Visit (SIV) agenda.
  • Conveys the Study Manager's perspective during the review of study documentation (e.g., Monitoring Guidelines).
  • Represents Lead Trial Managers or Study Managers in Study Management Teams and meetings.
  • Takes responsibility for reviewing reports (SQV, SMV, SCV) for sites assigned to other Study Managers within the same trial.
  • Assists in the development of country budgets and/or contract negotiations in collaboration with CCS colleagues.
  • Provides support with Audit Site Visits (ASV).
  • Metrics and Key Performance Indicators: The metrics and KPIs governing these services are detailed in the Quality Oversight Plan (QOP) document.


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