PhD to CTM: Associate Oncology Clinical Trial Manager

Medpace

Melbourne

Hybrid

AUD 90,000 - 130,000

Full time

14 days+

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Benefits offered by this job

Competitive compensation
Comprehensive health benefits
Paid time off
WFH flexibility after training
Mentorship and career development

Job summary

Medpace is seeking an Associate Clinical Trial Manager in Melbourne, Australia, for full-time employment. The role supports Project Coordinators and Clinical Trial Managers, applying analytical and academic skills to clinical project administration within a CRO environment.

Ideal candidates hold a PhD and Oncology experience, with strong English and presentation skills. This is a fast-paced, international team that values growth, training, and a defined career path in clinical trial management.

Qualifications

  • PhD in Life Sciences required.
  • Oncology experience advantageous.
  • Fluent English with solid presentation skills.
  • Ability to work in a fast-paced, international team.
  • CRO/pharma experience not required but advantageous.
  • Excellent computer, organizational and communication skills.

Responsibilities

  • Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager.
  • Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy.
  • Compile and maintain project-specific status reports within the clinical trial management system.
  • Interact with the internal project team, Sponsor, study sites, and third-party vendors.
  • Provide oversight and quality control of our internal regulatory filing system.
  • Provide oversight and management of study supplies.
  • Create and maintain project timelines; and
  • Coordinate project meetings and produce quality minutes.

Skills

English fluency
Presentation skills
Project coordination
Team collaboration
Computer skills

Education

PhD in Life Sciences

Job description

Medpace is seeking an Associate Clinical Trial Manager in Melbourne, Australia, for full-time employment. The role supports Project Coordinators and Clinical Trial Managers, applying analytical and academic skills to clinical project administration within a CRO environment.

Ideal candidates hold a PhD and Oncology experience, with strong English and presentation skills. This is a fast-paced, international team that values growth, training, and a defined career path in clinical trial management.

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