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Cra Ii
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Sydney, Australia ICON Full time**CRA II** **Location: Sydney, Melbourne, Brisbane** 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...
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Cra Ii
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Sydney, Australia Icon plc Full timeCRA II/ Senior CRA - home-based in Sydney/ Melbourne/ Brisbane/ Adelaide. Join us and advance your career with an industry leading CRO. ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to...
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Cra Ii
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Cra Ii
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Sydney, Australia Icon plc Full timeAt ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...
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Cra Ii
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Sydney, Australia Icon plc Full timeCRA II - Australia - Office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development Opening: CRA II (Australia) ICON plc is a world-leading...
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Cra Ii
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Cra Ii
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Sydney, Australia ICON Plc Full timeCRA II - Home-based in Australia ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II to...
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Cra Ii
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Sydney, Australia ICON Plc Full timeCRA II - Home-based in Australia ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II to...
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Senior CRA II – Hybrid Monitoring Leader
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Council of the City of Sydney, Australia Allucent Full timeA biopharmaceutical company in Australia is seeking a Clinical Research Associate (CRA II) to manage and monitor clinical trials, with responsibilities including site management and ensuring compliance with regulations. The ideal candidate has at least 2 years of onsite monitoring experience, preferably in oncology. The role offers a hybrid work environment,...
Cra Ii
3 weeks ago
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
The Role:
- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation.
- Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions.
- Balancing sponsor generated queries.
- Taking responsibility for study cost efficiency.
- Preparation and review of study documentation and feasibility studies for new proposals.
- Potential to assist in training and mentoring fellow CRAs.
You Will Need:
- 18 months+ of monitoring experience in phase I-III trials as a CRA (Oncology experience highly desirable, but not essential).
- College degree in medicine, science, or equivalent.
- Previous monitoring experience in medium-sized studies, including study start-up and close-out.
- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data.
- Excellent written and verbal communication.
- Ability to work to tight deadlines.
- Availability to travel upto 40% of the time (international and domestic -fly and drive) and should possess a valid driving license.
Benefits of Working at ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON 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, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.