Contract Clinical Trial Manager, Oncology

Category: CTM
Job #: 10946
Utilization: 100%
Location: Strong preference to be in Minnesota, Remote will be considered
Job Type: 1099
Therapeutics: Oncology

Our client, a global medical device leader in the oncology space, is seeking a Contract Clinical Trial Manager, Oncology to lead cross-functional clinical teams executing Phase II-III pivotal oncology trials. This is a contract opportunity with a preferred preference that you are based out of Minneapolis, but open to candidates anywhere in the United States to be fully remote candidates, supporting a growing portfolio focused on less invasive treatments for cancer patients. Job requirements and preferences listed below. If you are a fit, apply below!

Job Responsibilities:
  • Leads and directs cross-functional project teams in planning, executing, and managing all operational aspects of clinical oncology trials
  • Directs and executes global clinical studies in alignment with strategy, project plans, approved budgets, and applicable regulatory requirements
  • Collaborates with the project team on internal and external study materials, processes, plans, and regulatory submissions
  • Builds and maintains relationships with external physicians and key opinion leaders
  • Owns overall clinical trial project budget, including monthly maintenance, variance review, forecasting, and strategic planning
  • Provides direction and oversight to CROs and other clinical vendors
  • Ensures the study team maintains continuous audit readiness
  • Leads proactive identification, assessment, and management of clinical study risks
  • Develops and delivers presentations on study progress, data, outcomes, and risks to leadership
  • Provides clinical input into product development activities, representing the clinical function on cross-functional product development teams
  • Requires domestic travel of approximately 10-25%
Job Qualifications:
  • Bachelor's degree and 5+ years of oncology-related work experience, or equivalent combination of education and experience is required, while working directly for a Sponsor or CRO
  • 1+ year of project/trial management experience, while working for CRO or Sponsor is required
  • 1+ years of project or clinical trial budget management experience
  • 1+ years of experience with Clinical vendors and outsourced operations is required
  • Solid tumor medical device and/or drug development experience is a strong preference
  • Experience managing global clinical trials is a strong preference
  • Experience working with engineering or product development teams is a strong preference
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