Overview

• Oversee all stages of clinical trials across a wide scope of therapeutic areas
• Full service CRO
• Remote / on-site hybrid role

About the company

Our client is a fast-growing CRO company. You will work across multiple therapeutic areas across all phases. Join a close kit team that emphasises support and valuing employee contribution.

About the opportunity

The CRA/SCRA will act as the primary link between the sites and the sponsor and will oversee all stages of trials from initiation through to close out.

Duties

• Prepare, organise, conduct and follow-up routine monitoring and close out visits as per relevant study plan
• Motivate and train investigators and site staff to ensure obligations in regard to study timelines
• Ensure compliance with ICH/GCP, study protocols and other applicable regulatory guidelines
• Oversee all ethics submissions and trial reporting
• Follow company SOP’s and adapt knowledge and processes as applicable to the therapeutic area
• Contribute to process improvements and protocol review

Minimum requirements

• Tertiary degree in life sciences or relevant subject
• At least 12 months independent monitoring experience
• Ideally experience working in a research institution or CRO
• In depth knowledge of ICH / GCP guidelines
• Highly organized with excellent communication skills
• Full Australian working rights

Culture

Highly dynamic CRO that is expanding its presence in the APAC region. Join a fast growing and innovative company that awards hard work.

How to Apply
Click apply or contact one of our consultants for a confidential discussion:

Davina Ocansey, Senior Recruitment Consultant on +61 2 8877 8712

Mattias Fitzgerald, Recruitment Consultant on +61 2 8877 8749