As the Sponsor representative, you will act as the lead monitor across an eight-site Phase IIa study, working closely with investigative sites and the CRO partner to provide senior-level oversight from site activation through to close-out, ensuring data quality, protocol compliance, and effective study execution.
This role is suited to a highly autonomous CRA who is comfortable operating independently, building strong site relationships, and exercising sound judgement on study and site issues.
About You
- Solid years' CRA monitoring experience, including Phase II studies.
- Strong knowledge of ICH-GCP and the ANZ clinical trial landscape.
- Able to work independently and confidently manage site issues and escalations.
- Life Sciences, Nursing, Pharmacy or related qualification.
- Willingness to travel across Australia and New Zealand.
- Flexible independent contractor engagement.
- Competitive day rate.
- Opportunity to work directly with senior clinical leadership.
- Exposure to an innovative respiratory development program with a growing biotech organisation.
