Clinical Trial Manager, Oncology Job Description

Clinical Trial Manager, Oncology Job Description Template

Our company is looking for a Clinical Trial Manager, Oncology to join our team.

Responsibilities:

  • Assist PM with preparation of information for inclusion in monthly report to client;
  • Define the scope of work with the client and clinical monitoring team;
  • Assist PM in identifying and generating changes in scope and notify client of potential changes in scope;
  • Assist PM in review of project budgets, monitoring costs, potential overruns and propose/implement cost effective solutions;
  • Assist PM in preparation of audit responses, as appropriate;
  • Serve as client advocate within IQVIA Biotech;
  • Review and approve CRA travel expenses and time sheets;
  • Ensure all project documentation is appropriately filed per IQVIA Biotech SOPs;
  • Develop and implement Clinical Monitoring Plan;
  • Assure that the appropriate IQVIA Biotech and/or sponsor SOPs are followed.

Requirements:

  • Ability to manage 2 studies at once;
  • 2+ recent years of experience working on Oncology trials;
  • Knowledge of ICH-GCP;
  • Experience with global studies;
  • 3-5+ recent years working as a Clinical Trial Manager;
  • Bachelor’s degree or higher in related scientific subject;
  • Phase 1 Dose Escalation experience.