Your new role

• Site selection, initiation, monitoring and close out visits across sites located mainly in Sydney and Melbourne.
• Conduct all clinical site activities according to the monitoring plan and in accordance with the study timelines across multiple early phase Oncology protocols.
• Work closely with the sponsor of each study and ensure all trial related activities are met in accordance with ICH GCP.
• Interact and build professional and collaborative relationships with all study personnel (investigator, study coordinator, pharmacist) and peers.
• Create and submit all regulatory and ethics documents.
• Attend and support investigator meetings.
• Where required, assist in site and CRO audits.
• Reporting directly to the Country Head.

What you'll need to succeed

• Full working rights in Australia.
• 3 years independent monitoring experience in Australia and/or New Zealand.
• Previous experience in Phase I Oncology trials, ideally within a CRO setting.
• Availability to travel interstate.
• Bachelor's degree within a Life Sciences field.
• Ability to work autonomously.

What you'll get in return

• Work from home (home-based)
• Warm culture
• Good teamwork environment
• Competitive salary ($115k to $125k Base + $15k Car Allowance + Super + Bonus depending on experience)
• Work with mid-size pharmaceutical sponsors from Europe, US, Asia, and Japan

What you need to do now

If you're interested in this role, click 'apply now' or forward an up-to-date copy of your CV to maria.martinezdaza@hays.com.au, or call us now on +61 (0)2 8860 1601.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.