Senior Project Manager

Are you passionate about making a positive and impactful difference to the lives of others through Clinical Research? Join Alexion as a Senior Project Manager.  

About Alexion, Astra Zeneca Rare Disease
At Alexion, we’re dedicated to delivering life-changing medicines for those with rare and devastating diseases. Our patient first approach informs all our decision-making, and we invest in team and individual development. Ours is an energetic, fast-paced way of working that is solutions focused and collaborative.

We will help you expand your skills and knowledge and unlock your best. Working at pace, you’ll be challenged and supported to grow – learning from inspiring leadership and exceptional teams who believe in the power of science to make a difference. Every day you will broaden your horizons and skills, finding opportunities to take the initiative and build a meaningful career. Our outstanding learning resources and new diverse career-enhancing opportunities will quickly deepen your personal and professional growth.

About the role
Join us at Alexion, AstraZeneca Rare Disease, as a Senior Project Manager, responsible foreffective and proactive study management across several studies. As such, this is a broad role where you will have high level of involvement across all stages of the studies from study feasibility through to close.   You will have the opportunity to embrace new challenges and advance your career as our Clinical Operations team continues to expand.

This role is a full time, permanent position to be based from Sydney.

Requirements

• Tertiary qualifications in a field related to clinical practice, healthcare, life sciences, or drug development.

• At least 4 years of relevant experience with a CRO or pharmaceutical company on multinational clinical studies

• Proven experience managing high-priority/complex studies through phases 1–4, with preference for trials involving rare medical conditions.

• Strong knowledge of clinical development processes, GCP, and local regulations, with a track record of ensuring GCP compliance and managing risks in complex studies.

• Ability to lead, troubleshoot, and influence for quality and delivery.

• Proven experience communicating effectively with site staff, including KOLs and thought leaders.

• Experience or interest in people leadership, team management, and coaching/developing CRAs.

Why Alexion?  

At Alexion, people living with rare and devastating diseases are our Guiding Star. We are driven to continuously innovate and create meaningful value in all we do to help patients and families fully live their best lives. We value the uniqueness and diversity of our employees and recognize that nurturing the diverse perspectives and strengths of our people translate into innovative breakthroughs for patients.  

We want to unlock your potential and inspire you to be your best, challenging you to expand your horizons, extend your knowledge, and grow to your fullest.

So, what’s next?

• Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it’s yours!

• If you’re curious to know please reach out to Danielle Jones.
  

Where can I find out more?

• Our Social Media, Follow AstraZeneca on LinkedIn
• Visit our websites https://www.astrazeneca.com.au/careers.html and https://www.astrazeneca.com/
• For some useful hints and tips, please visit https://careers.astrazeneca.com/application-hints-tips

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.