External Title Director, Clinical Trial Management - Oncology
Medpace is continuing to expand our global Clinical Trial Management team and is seeking an experienced Director, Clinical Trial Management to lead complex global clinical trials while developing and mentoring high-performing project management teams.
This is a strategic leadership role focused on both people leadership and operational execution.
The ideal candidate is a strong leader who thrives in a fast-paced CRO environment, enjoys mentoring and developing talent, and has a passion for building collaborative, high-performing teams.
This role offers the opportunity to influence organizational strategy, lead large-scale and high-profile studies, and contribute directly to advancing innovative therapies.
Responsibilities
Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
Serve as primary Sponsor contact for operational project-specific issues and study deliverables
Maintain in depth knowledge of protocol, therapeutic area, and indication
Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
Develop operational project plans
Manage risk assessment and execution
Manage study vendors where applicable
Manage site quality and monitoring deliverables
Qualifications
Bachelor's degree in a health-related field; Advanced degree in a health-related field preferred




Experience in Phases 1-4; Phases 2-3 preferred
5+ years as a project/clinical trial manager within a CRO
Management of overall project timeline
Strong leadership skills
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO).
We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.
Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.
We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?
People.
Purpose.
Passion.
Make a Difference Tomorrow.
Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas.
The work we do today will improve the lives of people living with illness and disease in the future.
Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for skilled growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies in ****, ****, **** and ****
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
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📌 External Title Director, Clinical Trial Management - Oncology (Melbourne)
🏢 Medpace
📍 Melbourne