Senior Clinical Research Associate - FSP

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 SCRA or PCRA 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:

SCRA/PCRA

• Requires at least 4 years monitoring experience

• You must have full 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