About Avance Clinical Avance Clinical is a full-service CRO for biotechs with a proven track-record for delivering clinical excellence in Australia, New Zealand, Asia, North America and Europe. Avance Clinical specializes in delivering top-tier clinical trials that yield globally accepted data. Award-winning CRO for Biotechs Avance Clinical has been recognized for the fourth consecutive year by Frost & Sullivan in 2023, being awarded the Best Practices Customer Value Leadership for Biotech’s award, for its continuous exceptional performance. Pre-clinical through to Phase I and Beyond Avance Clinical offers pre-clinical consultancy services with their experienced ClinicReady team right through to Phase I and beyond clinical services leveraging significant Government incentive rebates of up to 43.5% and rapid start-up regulatory processes that are available in Australia and highly qualified sites and networks within the United States. With experience across more than 120 therapeutic indications, Avance Clinical can deliver world-class, high-quality, internationally accepted data suitable for FDA and EMA review. Technology Avance Clinical uses state-of-the-art technology and gold-standard systems across all functional areas to provide clients with the most effective processes. Medidata, Oracle, Zelta, Veeva and Medrio are just some of Avance Clinical’s technology partners. www.avancecro.com

Job description

We’re Avance Clinical a Contract Research Organization. We offer specialized services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980’s. If you already work in this industry, you’ll know that we are experts in our field.

Responsibilities

The Contract Clinical Research Associate (cCRA) performs activities associated with the evaluation, initiation, monitoring and close out of clinical trials to ensure the trial is conducted in accordance with the protocol; company Standard Operating Procedures (SOPs), ICHGCP guidelines and other applicable regulatory requirements.

What We Offer

Stimulating work
Project diversity
An intellectual challenge
An agile & flexible workplace
Opportunity to progress
Stability
Sense of community
A leadership team that are working together on a common goal
Flexible work options
Great tools / tech to do your job

Qualifications, Skills and Experience

Bachelor’s level degree in life sciences, pharmacy, nursing or appropriate industry experience.
At least 12 months experience in the pharmaceutical industry / CRO working in clinical project management
Formal ICH GCP training (desirable).
Well developed knowledge of ICH GCP Guidelines and other applicable regulatory requirements.

Required profile