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May

Senior Cra | Australia Wide

ICON plc - Sydney, NSW

Health, Medical & Pharmaceutical
Source: uWorkin

JOB DESCRIPTION

Clinical Research Associate (All Levels Of Experience)

Location: Sydney, Melbourne, Brisbane, Adelaide, Perth

  • Therapeutic Experience in Oncology and Vaccine advantageous
  • Career progression and growth; exposure to mentorships and even access to management training programs!
  • Open to all levels of experience and across Australia
  • Work Visa sponsorships can be discussed
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.

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. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

We offer a world class learning platform that would aid in your professional and personal development! Working closely in a team and with your managers, you will be supported throughout your career development and for those inspiring Project or People Managers, we offer management training programs to prepare you for the next step in your career!

The Role
  • Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
  • Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
  • Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
  • Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
  • Dependent on level of experience you may assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects

What You Need
  • 18 months+ of monitoring experience in phase I-III trials as a CRA
  • Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
  • You will possess excellent written and verbal communication in English
  • Ability to produce accurate work to tight deadlines within a pressurized environment
  • You will be asked to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license

Benefits Of Working In 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.

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.

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 through the form below.

Sydney, NSW

Health, Medical & Pharmaceutical




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