Associate CTM: Global Clinical Trials & Flex Work

Medpace; Melbourne; On-site; AUD 90,000 - 150,000; Full time

Benefits offered by this job

Competitive compensation

Health, retirement, and PTO benefits

WFH after training

Job summary

Medpace is seeking a full-time Associate Clinical Trial Manager in Melbourne, Australia. The role supports project coordinators and CTMs in clinical trial administration, requiring a PhD or post-doctoral research background in relevant life sciences fields.

The candidate will engage with global teams, ensure timely tasks, and contribute to regulatory and project workflows. This entry-level opportunity offers intensive training, international exposure, and a pathway into Clinical Trial Management

Qualifications

• PhD in Life Sciences required.
• Research experience in cardiovascular, renal, metabolic or GI areas.
• Fluency in English with strong presentation skills.
• Ability to work in a fast-paced, international team.
• CRO/pharma experience not required but advantageous; strong IT skills.

Responsibilities

• Communicate and collaborate on global study activities with project teams.
• Ensure timely delivery of tasks with high accuracy.
• Compile and maintain project status reports in CTM systems.
• Interact with Sponsor, study sites and vendors; oversee regulatory filing system.
• Oversee study supplies and create/maintain project timelines; coordinate meetings.

Skills

English fluency

Presentation skills

Communication skills

Team collaboration

Computer skills

Education

PhD in Life Sciences

Tools

Word processing

Databases

Excel

Windows

Job description

Medpace is seeking a full-time Associate Clinical Trial Manager in Melbourne, Australia. The role supports project coordinators and CTMs in clinical trial administration, requiring a PhD or post-doctoral research background in relevant life sciences fields.

The candidate will engage with global teams, ensure timely tasks, and contribute to regulatory and project workflows. This entry-level opportunity offers intensive training, international exposure, and a pathway into Clinical Trial Management