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Oncology Trials Specialist

3 weeks ago

Halifax, Nova Scotia, Canada ICON Strategic Solutions Full time
Key Responsibilities
  1. Oversight of multiple oncology trials
  2. Leadership and mentorship to junior team members
  3. Acting as Lead Site Manager, training and guiding other site managers
  4. Representing Site Managers in key meetings
  5. Reviewing reports for assigned sites
  6. SUPPORTING country budget development
  7. Maintaining compliance with Metrics/KPIs

Requirements include:

  • At least 2 years of experience monitoring clinical trials in the pharmaceutical industry, preferably in oncology
  • Knowledge of risk-based/analytical monitoring approaches
  • Proficiency in clinical trial systems such as CTMS, EDC, TMF, IWRS, and safety reporting tools
  • Ability to actively drive patient recruitment strategies
  • Strong collaboration with investigators and site staff
  • In-depth understanding of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements

Applicants must be legally authorized to work in Canada and not require sponsorship for employment visa status.