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Senior Oncology Clinical Research Associate

2 months ago

Reston, Virginia, United States ICON Strategic Solutions Full time
Key Responsibilities

As a Senior Oncology Clinical Research Associate, you will be responsible for leading multiple oncology trials, focusing on quality of life with regional travel. You will demonstrate leadership through involvement in specific initiatives and serve as a subject matter expert (SME) to systems and processes.

  • Lead multiple oncology trials, ensuring quality of life is a primary focus.
  • Develop and implement site startup documents, including SIV agendas.
  • Provide SME input on study documents, such as Monitoring Guidelines.
  • Represent LTMs or SMs on SMTs and meetings.
  • Take over LTM role reports review for sites assigned to other SMs from the same trial.
  • Support country budget development and contract negotiation with CCS colleagues.
  • Assist with ASV and metrics/KPIs outlined in the Quality Oversight Plan (QOP) document.
Requirements

You must have 3 years of independent monitoring experience and oncology experience. You will be responsible for mentoring/coaching junior flex team members and training other SMs on study protocols.