Clinical Research Associate II/III - Melbourne

Novatech; Melbourne; Hybrid; AUD 80,000 - 120,000; Full time

Benefits offered by this job

Flexible working hours

Hybrid working arrangements

Career progression opportunities

Mentoring from leaders

Job summary

Novotech is seeking a Clinical Research Associate II/III in Melbourne to monitor sites, ensure safety and data integrity, and foster strong partnerships with investigators and sponsors.

The role offers flexible hours with hybrid working and clear internal career progression across Early Clinical Development and Phase I–III programs. A proactive mindset and passion for clinical research are essential.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, Health Sciences or related discipline.
• Strong communication and relationship-building skills.
• Sound knowledge of ICH-GCP and clinical trial conduct.
• Proactive, solutions-focused mindset.
• Passion for clinical research and improving patient outcomes.
• Australian Citizen or Permanent Resident.

Responsibilities

• Independently manage and monitor assigned sites.
• Use critical thinking to guide delivery of projects.
• Build strong relationships to partner with investigators and site personnel.
• Drive site performance and patient recruitment.
• Have strong support from IHCRA and Regulatory Start-Up teams.

Skills

Communication

Relationship-building

ICH-GCP knowledge

Proactive mindset

Clinical research passion

Education

Bachelor’s degree in Life Sciences or related

Job description

Clinical Research Associate II/III - Melbourne

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 II and CRA III 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.

Our continued growth has created exciting opportunities for career development and internal progression. We are proud of our track record of promoting from within and creating new opportunities for our people as we expand. Supporting career growth isn't just something we talk about—it's a genuine passion of our Clinical Operations leaders.

Biotech can be fast-moving, dynamic and highly collaborative. Our CRAs work closely with sponsors who value expertise, proactive problem-solving and genuine partnership. If you enjoy working in an environment where your contribution is recognised, your opinion is valued and your work has a direct impact on study success, Novotech offers a unique opportunity.

Why Join Novotech?

• Flexible working hours and hybrid working arrangements
• Monthly office calendar for social, wellbeing and team events that keep us connected.
• Opportunities across Early Clinical Development and Phase I-III programs
• Clear internal career pathways and promotion opportunities
• Leaders who are passionate about mentoring and developing their teams
• A culture where ideas, innovation and continuous improvement are encouraged

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 II

• Requires at least 6 months independent monitoring experience

CRA III

• Requires at least 2 years independent monitoring experience

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
• Be an Australian Citizen or Permanent Resident

You must have unrestricted working rights in Australia. Unfortunately, sponsorship is not available for this role.