Project Director (Early Phase), Australia

About the Opportunity

Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies.

With over 25 years of experience and a world-renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.

Global Expertise. Local Insight. Real Impact.

Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes.

Our 800+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.

About the Role

The Project Director (Early Phase) is responsible for oversight and supervision of all aspects of project delivery for an assigned portfolio of Early Phase projects – this portfolio may include local, regional and global clients and/or projects. Additionally, the role may include, but is not limited to, line management, acting as a Subject Matter Expert (SME) for an assigned topic, and supporting business development related activities.

Responsibilities

• Coordinate progress reporting for senior management, stakeholders, and clients
• Conduct internal Monthly Project Reviews, and escalate issues as needed
• Ensure project resource needs are identified and requested by Project Managers in a timely manner
• Oversee delivery of projects in line with customer and Emerald Clinical requirements, processes, and contracts
• Drive consistency, efficiency, and quality across projects
• Act as internal and client escalation point for key project issues

About You

Tertiary qualifications in a related science or health care discipline preferred – candidates without tertiary qualifications but with significant industry experience may be considered. Extensive experience in clinical trials, including experience with early-phase studies (Phase I/II), with approximately 10+ years of relevant experience, including a minimum of 5 years in project management, preferred. Line management experience desirable but not mandatory.

Why Join Us?

At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.

What We Offer

• Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience
• Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role
• Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role
• Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events
• Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients

Interested? Apply now and help us achieve our mission to improve the health of millions worldwide. We are an equal-opportunity employer and encourage applications from all qualified candidates.