Associate Clinical Trial Manager

Overview

Medpace, a leading CRO for Biotech companies, is seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager position in Melbourne, Australia. This role supports Project Coordinators and Clinical Trial Managers in clinical project management activities.

Responsibilities

• Communicate and collaborate on global study activities with project teams.
• Ensure timely delivery of recurring tasks with accuracy.
• Compile and maintain project-specific status reports in the management system.
• Interact with internal teams, sponsors, study sites, and vendors.
• Oversee and perform quality control for regulatory filing and study supplies.
• Create and maintain project timelines and coordinate meetings.

Qualifications

• PhD in Life Sciences with experience in Infectious Disease.
• Fluency in English and strong presentation skills.
• Ability to work in a fast-paced international environment.
• Excellent computer skills including Word, Excel, databases, and Windows.

Medpace Overview

Medpace is a full-service clinical CRO providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace accelerates global development of safe and effective therapeutics.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with professional growth
• Company-sponsored employee events and wellness initiatives

Key skills/competency

• Clinical Trials
• Project Management
• Communication
• Coordination
• Regulatory Oversight
• Data Analysis
• Clinical Research
• Quality Control
• Timeline Management
• Team Collaboration