Senior Clinical Research Associate

Senior Clinical Research Associate

Location: Home-based (Australia), ideally in Sydney or in Melbourne

As a Senior Clinical Research Associate, you will be joining the world’s largest & most comprehensive Clinical Research organisation, powered by healthcare intelligence.

With the support of ICON right behind you, you will be joining an innovative Biotech company, as one of the first CRAs in Australia with a vision to grow the team further in 2024 and 2025.  With a mission to develop, manufacture and commercialize high-quality medicines for the treatment of cancer and other major diseases, you will be working on first-in-class Oncology trials. You will not only have the opportunity to be part of a brand new team, but you will also have the opportunity to work on the full lifecycle of a trial, being involved from site identification, initiation through to close-out. This is a challenging career path that will support your growth and professional development and will broaden your expertise as a trial monitor. 

What you will be doing:

• Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock. 
• Lead site identification and initiation activities in Australia. 
• You will be embedded in our client's study team and have a dedicated ICON line manager to support you
• Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports

You are:

• Degree in Pharmacy or any related course 
• 4+ years prior monitoring experience with global trials in oncology
• Working experience with initial Australian ethics and regulatory submissions
• Excellent communication skills
• Excellent knowledge of international guidelines ICH-GCP, good knowledge of local regulations
• Flexibility to travel for monitoring visits as required 

Why ICON?

At ICON, we embrace new perspectives and empower our people to write their own paths forward. We are a culturally diverse company with over 40,000 talented and ambitious people with varied skills, perspectives & backgrounds working together across 40 countries.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.