Clinical Trial Jobs at Medpace, Australia
Medpace is hiring an experienced Clinical Trial Manager (CTM) to lead global and regional neuroscience/CNS clinical trials from its Melbourne office. This senior-level role offers the opportunity to manage complex, multiservice clinical studies end-to-end while collaborating with sponsors, investigators, and cross-functional global teams. The Clinical Trial Jobs at Medpace are ideal for professionals with CRO experience. This role places you at the forefront of ICH-GCP–compliant clinical trial execution in a scientifically driven organization.
Job Details:
- Job Title: Clinical Trial Manager (Neuroscience/CNS)
- Job ID: 11398
- Location: South Yarra, Melbourne, Australia
- Job Type: Full-time, Office-based
- Department: Clinical Trial Management
- Therapeutic Area: Neuroscience / Central Nervous System (CNS)
- Industry: Clinical Research, CRO
About the Company:
Medpace is a global, full-service Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies. Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 professionals across 40+ countries. Known for its scientifically led, disciplined approach, Medpace supports clinical development across multiple therapeutic areas, including CNS, oncology, cardiology, metabolic disease, endocrinology, and infectious diseases.
Educational Requirements for the Clinical Trial Manager Role:
- Bachelor’s degree or higher in a health or life sciences–related field
- Advanced degrees are considered an advantage
Key Responsibilities of the Clinical Trial Manager:
- Lead and manage day-to-day clinical trial operations in accordance with ICH-GCP and regulatory requirements
- Serve as the primary sponsor contact for project deliverables and study execution
- Maintain in-depth knowledge of the study protocol, indication, and therapeutic area
- Provide cross-functional leadership across clinical operations, data management, and vendors
- Develop and manage operational project plans, timelines, and risk mitigation strategies
- Oversee site quality and directly supervise Clinical Research Associates (CRAs)
- Manage study vendors and external partners
- Review and contribute to protocols, data analysis plans, edit check specifications, and final study reports
- Support bid defense meetings and business development activities
Skills Required for the Clinical Trial Manager Role:
- Strong expertise in global clinical trial management
- Solid understanding of ICH-GCP, regulatory requirements, and CNS trials
- Excellent leadership and cross-functional coordination skills
- Strong risk management and problem-solving abilities
- Effective stakeholder management and sponsor communication
- High level of organization, accountability, and adaptability
- Fluent written and verbal English communication skills
Benefits of the Clinical Trial Jobs at Medpace:
- Leadership role in global neuroscience/CNS clinical trials
- Competitive compensation and comprehensive benefits package
- Flexible work environment
- Structured career development and long-term growth opportunities
- Competitive paid time off (PTO)
- Employee health and wellness initiatives
- Company-sponsored appreciation and engagement events
- Opportunity to work in a scientifically driven, globally recognized CRO
