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Senior Clinical Trial Manager - Oncology (Home-based)

JR061459

About the role

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Clinical Trial Manager - Oncology
Home Based anywhere in US
  • As a CTM you would be expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
  • Primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients
  • Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects
  • Contribute to the development and maintenance of cross functional project management plans
  • Responsible for risk mitigation strategies, associated action plan and issue resolution
  • Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff
  • Provide direction and support to the Clinical Operations study team
  • Collaborate with Business Development (BD) to ensure timely completion of change orders
  • Track Clinical Operations project deliverables using appropriate tools
Role Requirements
  • Must have Clinical Trial Manager experience in Oncology
  • University/Bachelor's Degree in medicine, science or equivalent degree/experience.
  • A satisfactory progression of monitoring experience with previous experience in leadership and/or management activities
  • Previous working experience within the clinical trial management field.
  • Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials.
  • Some knowledge of project management processes and tools.
  • Fluent in written and spoken English.
  • Computer literate.
  • Due to the nature of this position it may be required for the employee to travel approx 25%. Therefore, dependent on the employee's location, the employee may be required to possess a valid Driver's license
List #1

Day in the life

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25 Years in Clinical Operations at ICON: Ricardo Cortizo Justo Q&A

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Our People

Content type

Blogs

Publish date

04/08/2026

Summary

Ricardo Cortizo Justo, Director of Clinical Operations and Site Head for Paris at ICON plc, recently marked an exceptional milestone of 25 years with the organisation. Over the course of his career, R

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Ricardo shares insights from 25 years at ICON, covering clinical operations, leadership, and career development.

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Central Monitoring vs On Site Monitoring

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Industry

Content type

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Publish date

04/03/2026

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Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re

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Learn the difference between central monitoring and on site monitoring and how both support patient safety and data quality.

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Francis' Journey back to ICON

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Our People

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03/26/2026

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Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February

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Francis Kayamba shares what drew him back to ICON and how the sponsor-embedded model works.

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