At Novotech, you'll work with innovative biotech and pharmaceutical sponsors who are deeply invested in their science and passionate about their molecules. As we continue to grow across Early Clinical Development and Phase I-III studies, we're looking for experienced CRA III and SCRA professionals to join our team.

We recognise that great CRAs want more than another monitoring role. They want supportive leadership, flexibility and a team where they feel valued. At Novotech, your line manager knows who you are, understands your career aspirations and is committed to helping you succeed. Our employee engagement surveys consistently show high levels of trust and respect between people leaders and their teams. You're not simply a number on a resource plan, you're a respected member of a collaborative, high-performing team where your ideas are welcomed, your opinion matters and your contributions help shape how we work.

This role will be based from QLD, NSW or VIC.

What You'll Be Doing

As a CRA, you will play a critical role in ensuring clinical trials are conducted safely, ethically and efficiently while building strong partnerships with investigators, study coordinators, pharmacists and sponsors.

You will:

- Independently manage and monitor assigned sites
- Use critical thinking to guide delivery of assigned projects
- Build strong relationships to partner with investigators and site personnel
- Drive site performance and patient recruitment
- Have strong support from dedicated IHCRA and Regulatory Start-Up teams
- Partner with sponsors and internal teams to successfully deliver clinical trials
- Protect participant safety and ensure the quality and integrity of clinical trial data

What We're Looking For:

CRA III

- Requires at least 2 years independent monitoring experience
- SCRA requires at least 4 years monitoring experience




- You must have experience in SSU including SIVs to be considered for this opportunity

You will also have:

- A Bachelor’s degree in Life Sciences, Nursing, Pharmacy, Health Sciences or a related discipline
- Strong communication and relationship-building skills
- Sound knowledge of ICH-GCP and clinical trial conduct
- A proactive, solutions-focused mindset
- A passion for clinical research and improving outcomes for patients

Novotech is a global full-service clinical Contract Research Organization (CRO).

At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of the industry with an award-winning workplace culture that values ambition, innovation, and growth. Named Employer of Choice, Great Place to Work and Employer of Choice for Gender Equality (EOCGE), we are committed to fostering an environment that reflects the life-changing work we do.

Since 1997, we have expanded our global footprint, now with 30+ offices across Asia-Pacific, the United States, and Europe. This growing network unites professionals from diverse backgrounds and disciplines to advance therapies that improve patient outcomes worldwide.

At Novotech, our employees are at the heart of our success. By offering trust, flexibility, and autonomy through programs like NovoLife, our flexible benefits framework, we empower team members to create an effective work-life balance that delivers professional satisfaction and maximum results for clients.

With access to mentorship opportunities, professional development programs, and a agile community, Novotech offers a platform for driven individuals to achieve personal growth while shaping the future of healthcare. Join us to be a part of a team that values your contributions and supports your ambition to make a global impact.

📌 Senior Clinical Research Associate - FSP (Australia)
🏢 Novotech
📍 Australia