Senior Clinical Research Associate (Contract)

On Q Recruitment; Sydney; Presencial; AUD 166 000 - 221 000; Tempo parcial

Vantagens oferecidas por esta oferta de emprego

Flexible contractor engagement

Competitive day rate

Direct exposure to senior leadership

Respiratory biotech program exposure

Resumo da oferta

On Q Recruitment client, a clinical-stage biotech, seeks a Senior Clinical Research Associate to support a Phase II respiratory study across Australia and New Zealand. As sponsor representative, you will lead monitoring at eight sites from site activation through close-out, ensuring data quality, protocol compliance and smooth study execution.

The role suits a highly autonomous CRA who can build strong site relationships, manage escalations, and travel as required to AU/NZ.

Qualificações

• 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.

Responsabilidades

• Act as lead monitor across eight sites from activation through close-out.
• Ensure data quality and protocol compliance throughout the study.
• Collaborate with investigative sites and CRO partner to execute the study.
• Provide senior-level oversight and effective issue resolution at sites.

Conhecimentos

CRA monitoring experience

Phase II experience

ICH-GCP knowledge

Independent site management

Travel willingness

Formação académica

Life Sciences / Nursing / Pharmacy related qualification

Descrição da oferta de emprego

Our client, a clinical-stage biotech company, is seeking an experienced Senior Clinical Research Associateto support a Phase II respiratory study across Australia and New Zealand.

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.

What's on Offer

• 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.