Clinical Research Associate II/III - Brisbane

Novotech; Brisbane; Hybrid; AUD 85,000 - 120,000; Full time

Benefits offered by this job

Hybrid working arrangements

Job summary

Novotech is seeking experienced CRAs to join our biotech-focused team in Australia. As a CRA II or CRA III, you will monitor sites, ensure ethical conduct, and drive patient recruitment across Early Clinical Development and Phase I-III studies.

You'll work with investigators, sponsors and IHCRA/Regulatory Start-Up teams, enjoying flexible hours and hybrid working arrangements. A life sciences degree and ICH-GCP knowledge are essential, with sponsorship not available for this role.

Qualifications

• Must have independent monitoring experience (CRA II: at least 6 months).
• Must have independent monitoring experience (CRA III: at least 2 years).
• Australian Citizen or Permanent Resident; unrestricted working rights in Australia; no visa sponsorship.

Responsibilities

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

Skills

Independent monitoring experience

Communication skills

Education

Bachelor’s degree in Life Sciences or related

Job description

Passionate about biotech? So are we.

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.

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
• The opportunity to work with sponsors who view Novotech as a true strategic partner

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

Eligibility

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