Study Start Up Associate II Location: Australia (home-based) ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
We are looking for an experienced Study Start Up Associate to join an exciting sponsor program based in Australia. This is a great opportunity for those with clinical trials site activation experience within CRO/ pharma in Australia, who are looking to pursue a career within a sponsor dedicated site start-up function.
You will be responsible for ethics and regulatory submission and all site initiations and activations, partnering with one of our global biopharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry, focusing on finding a cure to fight Cancer.
What you will be doing: You will be responsible for the complete start-up process to clinical trials from site feasibility, initiation through to site activation. You will take ownership of drafting Ethics Committee and regulatory submissions. Working directly with the sponsor's studies across a number of therapeutic areas means that this is a varied role with different challenges. You will have a focus on start-up activities across Australia and New Zealand. You will be part of a supportive global team with access to external training opportunities. ICON is committed to providing career development pathways and ongoing support. You are: Tertiary Degree qualified. Minimum 1-2 years of previous experience in clinical trial start-up in Australia within CRO/ Pharmaceutical or Biotechnology company. Thorough understanding of local clinical trials process and the ethics submission/ governance/ regulatory process. Genuine interest in the start-up process of clinical trials. You show yourself to be a talented communicator with excellent management of competing priorities. Full, unrestricted working rights in Australia. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
Our benefits examples include:
Various annual leave entitlements. A range of health insurance offerings. Competitive retirement planning offerings. Global Employee Assistance Programme. Life assurance. Flexible country-specific optional benefits. Visit our careers website to read more about the benefits of working at ICON:
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless.
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