Passionate about biotech? So are we.
At Novotech, you'll work with cutting-edge 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 team-oriented, 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.
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